5-Acetyl-2-hydroxybenzamide
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5-Acetyl-2-hydroxybenzamide
structure -
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CAS No:
40187-51-7
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Formula:
C9H9NO3
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Chemical Name:
5-Acetyl-2-hydroxybenzamide
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Synonyms:
Benzamide,5-acetyl-2-hydroxy-;5-Acetyl-2-hydroxybenzamide;5-Acetylsalicylamide
- Categories:
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CAS No:
Characteristics
80.4
1.6
Off white to yellowish crystalline powder
1.3±0.1 g/cm3
217 °C
395.6°C at 760 mmHg
181.4±25.1 °C
1.598
Safety Information
NONH for all modes of transport
3
20/21/22-36/37/38-22
26-36-37/39
CU8702280
Xn
P261-P280-P305 + P351 + P338
H302-H312-H315-H319-H332-H335
|Warning|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 45 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
5-Acetyl-2-hydroxybenzamide Use and Manufacturing
1), NaCl-AlCl3 low melting point mixed molten salt system preparation:A 100 ml three-necked flask, Mechanical agitation, Condensate tube (linked to tail gas HCl absorption device), 0 ~ 200 thermometer and constant pressure dropping funnel consisting of the device placed in a constant temperature oil bath;Quickly weighed 0.0648 mol (about 8.64 g) of anhydrous aluminum chloride, 0.0648 mol (about 3.79 g) of sodium chloride was added to the flask, Open the mechanical stirring, heating to 140 , The solid is melted and the temperature is stable.Note: After about 25 minutes, anhydrous aluminum chloride, sodium chloride are in a molten state.2), weigh 0.036 mol (about 5.00 g) of salicylamide under stirring to add the flask(Flask temperature 140 )And melted, The temperature inside the flask is stable.3), weighed 0.0432 mol (about 3.39 g) of acetyl chloride, With a constant pressure dropping funnel through the condenser tube into the system, About 10min drops finished.The temperature of the drop was maintained at 140 ° C for 0.5 h, The reaction is complete.which is, The reaction was carried out in a NaCl-AlCl3 low melting point mixed molten salt system as a solvent.4), immediately after the completion of the reaction within the system slowly (that is, even within 5 minutes evenly added)60ml acid (composed of 1ml concentrated hydrochloric acid and 59ml ice water mixture)Producing a pale yellow solid, After the addition of the acid solution, the stirring was continued for 30 min at room temperature.At this point no longer produce light yellow solid;Get the suspension.5), filter the suspension, To give a pale yellow solid, And washed three times with hot water at 80 ° C (5 ml each)Drying (80 ° C, drying for 5 h) yields the crude product.6), and the resulting crude product was added with 20 ml of ethanol, Heated to reflux temperature, The crude product is completely dissolved, After the re-crystallization in the ice bath, Precipitation of the crystal filter drying (80 , drying 5h), To give 5-acetylsalicylamide as a white solid(Purity ≥ 98.1percent), the yield was 92.2percent.
Used as a pharmaceutical intermediate, can be used to synthesize anti-allergic drugs and anti-inflammatory drugs
Computed Properties
Molecular Weight:179.17
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:179.058243149
Monoisotopic Mass:179.058243149
Topological Polar Surface Area:80.4
Heavy Atom Count:13
Complexity:227
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Recommended Suppliers of 5-Acetyl-2-hydroxybenzamide
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