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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531407Generated: October 30, 2026

Arsanilic Acid → [4-(2-Bromoacetamido)phenyl]arsonic acid

https://huagongshe.com/reaction/531407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantArsanilic AcidHCID 7389—
ReactantSodium CarbonateHCID 10340—
ReactantBromoacetyl bromideHCID 61147—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product[4-(2-Bromoacetamido)phenyl]arsonic acidHCID 193853—

Reaction Conditions

Temperature4 °C

Reaction Steps

BRAA was prepared by a modification of the method described in Donoghue et al (2000) and WO 01/21628. p-Arsanilic acid (20.6 g, 95 mmol) was added in portions to a solution of sodium carbonate (20 g, 189 mmol) in water (200 mL). When all solids had dissolved, the solution was found to be pH 10, and was chilled at 4° C. for 2 hours. Bromoacetyl bromide (15 mL, 173 mmol) in dry dichloromethane (35 mL) was added in two portions, each addition followed by vigorous shaking for 2 to 3 min. The mixture was allowed to stand for a few minutes, and the lower organic layer was drained off. 4-(N-(Bromoacetyl)amino)benzenearsonic acid (BRAA) was precipitated by acidification of the solution to about pH 2-3 with the dropwise addition of 98% sulfuric acid, collected by vacuum filtration, and dried, giving BRAA as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353152B2
Source datasetuspto-grants-2016_05
ORD IDord-3a8edfe38fa24a65b482489fe5117ed2
Source noteuspto-grants-2016_05