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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287794Generated: October 31, 2026

Benzyl Bromide → 3-Benzylamino-4-isopropylamino-5-sulphamyl-benzoic acid

https://huagongshe.com/reaction/1287794

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant3-Amino-4-isopropylamino-5-sulphamyl-benzoic acidHCID 21505990—
SolventEthanolHCID 702—
Product3-Benzylamino-4-isopropylamino-5-sulphamyl-benzoic acidHCID 21506028—

Reaction Steps

A mixture of 3-amino-4-isopropylamino-5-sulphamyl-benzoic acid (2.62 g), benzyl bromide (4.28 g), and anhydrous ethanol (25 ml) was refluxed for 24 hours. The reaction mixture was evaporated in vacuo. 1N sodium hydroxide (30 ml) was added, and the mixture was heated on a steam bath for 1 hour. After cooling and extracting with diethyl ether, the aqueous layer was adjusted to a pH of 3 by addition of a 4N hydrochloric acid. The precipitated 3-benzylamino-4-isopropylamino-5-sulphamyl-benzoic acid was collected by suction and recrystalized from aqueous ethanol. The melting point was 233°-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03985777
Source datasetuspto-grants-1976_10
ORD IDord-995f39cef23e4df9a0070e07fc1abe91
Source noteuspto-grants-1976_10