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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425235Generated: October 30, 2026

Hydrogen Bromide → N-((S)-3-bromo-2-hydroxypropyl)-5-chlorothiophene-2-carboxamide

https://huagongshe.com/reaction/425235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantMethanolHCID 887—
ReactantAcetic AnhydrideHCID 7918—
Reactant5-Chloro-N-((S)-2,3-dihydroxypropyl)thiophene-2-carboxamideHCID 9991690—
SolventAcetic AcidHCID 176—
ProductN-((S)-3-bromo-2-hydroxypropyl)-5-chlorothiophene-2-carboxamideHCID 10108741—

Reaction Conditions

Temperature62.5 °C

Reaction Steps

301.7 ml of a 33% solution of hydrobromic acid in acetic acid are added to a suspension of 100 g of N-((S)-2,3-dihydroxypropyl)-5-chlorothiophene-2-carboxamide (VIII) in 250 ml of glacial acetic acid at from 21 to 26° C. over a period of 30 minutes. Subsequently, 40 ml of acetic anhydride are added and the reaction mixture is stirred at from 60 to 65° C. for three hours. At 20 to 25° C., 960 ml of methanol are then added over a period of 30 minutes. The reaction mixture is stirred under reflux for 2.5 hours and then overnight at from 20 to 25° C. For workup, the solvents are distilled off under reduced pressure at approx. 95 mbar. The remaining suspension is admixed with 50 ml of 1-butanol and 350 ml of water. The precipitated product is filtered off with suction, washed with water and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106192B2
Source datasetuspto-grants-2012_01
ORD IDord-2cc01475d2b741888dc6133267712869
Source noteuspto-grants-2012_01