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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23824Generated: October 27, 2026

Formic Acid → 5-Bromo-2-chloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamide

https://huagongshe.com/reaction/23824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-bromo-2-chloro-N-(2-hydroxyamino-ethyl)-benzamideHCID 22590605—
SolventPyridineHCID 1049—
Product5-Bromo-2-chloro-N-[2-(N-formyl-N-hydroxy-amino)-ethyl]-benzamideHCID 2259061055%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of acetic anhydride (2 mL) and formic acid (1 mL) was allowed to stand at 55° C. for 2.5 h. After cooling to 0° C., the resulting mixed anhydride (0.5 mL) was added to a solution of 5-bromo-2-chloro-N-(2-hydroxyamino-ethyl)-benzamide (0.7 g, 2.4 mmol) in pyridine (6 mL) at 0° C. under an argon atmosphere. The reaction mixture was stirred for 1 h and the pyridine removed in vacuo. The residue was chased twice with water and twice with MeOH. The resulting solid was washed with ether/acetonitrile (9:1) to provide the title compound (0.42 g, 55%) as a white solid. 1H NMR* (400 MHz, CD3OD): δ 8.35 (s, 0.5H); 7.95 (s, 0.5H); 7.58 (m, 2H); 7.38 (m, 1H); 3.78 (m, 1H); 3.73 (m, 1H); 3.62 (m, 2H). * 1:1 mixture of rotamers. ESMS: M+H=321.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06852882B2
Source datasetuspto-grants-2005_02
ORD IDord-c9f97c0f5c424e51a9503dabfb0aca53
Source noteuspto-grants-2005_02