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Isomlamine and methyl acrylate to react through Hiffine?
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Koffi Seglo
Isomlamine and methyl acrylate to react through Hiffine?
It is impossible to react, or it is difficult to occur. When this ester is still present, the amino group is not likely to form a so-called Schiff base
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
It is impossible to react, or it is difficult to occur. When this ester is still present, the amino group is not likely to form a so-called Schiff base
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
Both reactions and product analog search results link: https://pan.baidu.com/s/1nubpv8hrqtv9adeew-qc_q extraction code: hug9, I hope to help you! The product is new compound, analog retrieval: 3 of 5 Similarity Candidates Selected Substances ≥ 99 (MOST Similar) 0 95-98 0 90-94 0 85-89 0 75-79 27 70-74 105 65-69 381 0-64 (Least Similar) 3265
Both reactions and product analog search results link: https://pan.baidu.com/s/1nubpv8hrqtv9adeew-qc_q extraction code: hug9, I hope to help you! The product is new compound, analog retrieval: 3 of 5 Similarity Candidates Selected Substances ≥ 99 (MOST Similar) 0 95-98 0 90-94 0 85-89 0 75-79 27 70-74 105 65-69 381 0-64 (Least Similar) 3265
It is impossible to react, or it is difficult to occur. When this ester is still present, the amino group is not likely to form a so-called Schiff base
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
It is impossible to react, or it is difficult to occur. When this ester is still present, the amino group is not likely to form a so-called Schiff base
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
Both reactions and product analog search results link: https://pan.baidu.com/s/1nubpv8hrqtv9adeew-qc_q extraction code: hug9, I hope to help you! The product is new compound, analog retrieval: 3 of 5 Similarity Candidates Selected Substances ≥ 99 (MOST Similar) 0 95-98 0 90-94 0 85-89 0 75-79 27 70-74 105 65-69 381 0-64 (Least Similar) 3265
Both reactions and product analog search results link: https://pan.baidu.com/s/1nubpv8hrqtv9adeew-qc_q extraction code: hug9, I hope to help you! The product is new compound, analog retrieval: 3 of 5 Similarity Candidates Selected Substances ≥ 99 (MOST Similar) 0 95-98 0 90-94 0 85-89 0 75-79 27 70-74 105 65-69 381 0-64 (Least Similar) 3265
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
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The product is new compound, analog retrieval:
3 of 5 Similarity Candidates Selected Substances
≥ 99 (MOST Similar) 0
95-98 0
90-94 0
85-89 0
75-79 27
70-74 105
65-69 381
0-64 (Least Similar) 3265
The product is new compound, analog retrieval:
3 of 5 Similarity Candidates Selected Substances
≥ 99 (MOST Similar) 0
95-98 0
90-94 0
85-89 0
75-79 27
70-74 105
65-69 381
0-64 (Least Similar) 3265
More
VOTE
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
in the carbonyl group
, the reaction is acylated, ester group leavingThus, the product is probably the product is likely to be a monoxylated and azocylated product, an intermediate amine (secondary amine) is difficult to acylate (under this conditions)
Further, the side reaction mayIncluding double bond addition, addition to amino group, under acidic conditions
esterlation, generally catalyzed with sodium carbonate, potassium carbonate, sodium alcohol, etc., the reaction can be continuously evaporated to promoteTurn to the direction of the product
More
VOTE
More
VOTE
The product is new compound, analog retrieval:
3 of 5 Similarity Candidates Selected Substances
≥ 99 (MOST Similar) 0
95-98 0
90-94 0
85-89 0
75-79 27
70-74 105
65-69 381
0-64 (Least Similar) 3265
The product is new compound, analog retrieval:
3 of 5 Similarity Candidates Selected Substances
≥ 99 (MOST Similar) 0
95-98 0
90-94 0
85-89 0
75-79 27
70-74 105
65-69 381
0-64 (Least Similar) 3265
More
VOTE
More
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