2,4-Dimethoxybenzenesulfonyl chloride
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2,4-Dimethoxybenzenesulfonyl chloride
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CAS No:
63624-28-2
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Formula:
C8H9ClO4S
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Chemical Name:
2,4-Dimethoxybenzenesulfonyl chloride
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Synonyms:
Benzenesulfonyl chloride,2,4-dimethoxy-;2,4-Dimethoxybenzenesulfonyl chloride;2,4-Dimethoxyphenylsulfonyl chloride;2,4-Dimethoxybenzene-1-sulfonyl chloride
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CAS No:
Safety Information
II
8
3261
3
34-43
45-36/37/39-3-26
C,Xi
Corrosive/Harmful/Moisture Sensitive
P280-P305 + P351 + P338-P310
H314-H317
|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P261, P264, P272, P280, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P333+P313, P363, P405, and P501|Aggregated GHS information provided by 42 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
2,4-Dimethoxybenzenesulfonyl chloride Use and Manufacturing
A solution of 2, 4-dimethoxybenzenesulfonyl chloride (0.052 g, 0.22 mmol) and 6-(methoxymethyl)-5-methylbenzo[d]isoxazol-3-amine I4 (0.042 g, 0.22 mmol) in pyridine (0.500 ml.) was irradiated in the microwave at 110 C for 2 hours. The resulting mixture was loaded onto silica gel and the product purified by column chromatography (4 g S1O2 cartridge, 0-45% EtOAc in petroleum benzine 40-60 C) to yield the title compound (0.0413 g, 48% yield) as a white solid. 1H NMR (400 MHz, CDCI3) d 7.96 (s, 1H), 7.83 (s, 1H), 7.71 (d, J = 8.33 Hz, 1H), 7.47 (s, 1H), 6.48 (d, J = 1.82 Hz, 1H), 6.42 (d, J = 8.36 Hz, 1H), 4.50 (s, 2H), 3.95 (s, 3H), 3.80 (s, 3H), 3.47 (s, 3H), 2.37 (s, 3H). LCMS-A: rt 5.78 min, m/z = 392.8 [M+H]+, 414.7 [M+Na]+.A solution of NaH (60% in mineral oil, 5 or 10 eq.) was added to a solution of 4-methoxybenzo[d]isoxazol-3-amine (100 mg, 0.609 mmol) in THF (5.0 ml.) and stirred at room temperature for 10 minutes. The sulfonyl chloride (1 eq., 0.609 mmol) was added and the reaction was stirred for 16 hours. The resultant mixture was loaded onto silica gel and purified by column chromatography (0-100% petroleum benzine 40-60 C then 0-60% MeOH in EtOAc) to yield the desired product.Example 148: N-(benzo[d]isoxazol-3-yl)-2, 4-dimethoxybenzenesulfonamide 148 A solution of 2, 4-dimethoxybenzenesulfonyl chloride (0.18 g, 0.75 mmol) and benzo[d]isoxazol-3-amine (0.10 g, 0.75 mmol) in pyridine (1 ml.) was irradiated in the microwave at 1 10 C for 2 hours. The resultant mixture was loaded onto silica gel and the product purified twice by column chromatography (4 g Si02 cartridge, 0-45% EtOAc in petroleum benzine 40-60 C then 4g Si02 cartridge, 0-35% EtOAc in petroleum benzine 40-60 C) to yield two batches (78 mg and 5 mg) of [183] the title compound (total mass 83 mg, 33 % yield) as white solids. 1H NMR (400 MHz, CDCI3) d 8.1 1 (d, J = 8.05 Hz, 1H), 7.79 (s, 1H), 7.70 (d, J = 8.81Hz, 1H), 7.57 - 7.50 (m, 1H), 7.47 - 7.40 (m, 1H), 7.37 - 7.29 (m, 1H), 6.50 (d, J = 2.27 Hz, 1H), 6.42 (dd, J = 2.25, 8.81Hz, 1H), 3.98 (s, 3H), 3.81 (s, 3H). LCMS-B: rt 3.20 min, m/z = 356.8 [M+Na]+, 334.8 [M+H]+.
Computed Properties
Molecular Weight:236.67
XLogP3:1.5
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:235.9910076
Monoisotopic Mass:235.9910076
Topological Polar Surface Area:61
Heavy Atom Count:14
Complexity:272
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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2,4-Dimethoxybenzenesulfonyl chloride
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