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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Arsanilic Acid | HCID 7389 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [4-(2-Bromoacetamido)phenyl]arsonic acid | HCID 193853 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09353152B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-3a8edfe38fa24a65b482489fe5117ed2 |
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| Source note | uspto-grants-2016_05 |
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