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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 841194Generated: October 25, 2026

Oxalyl chloride → (R)-N-[2-Bromo-4-(phenylthio)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamide

https://huagongshe.com/reaction/841194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant2,6-Di-tert-butylpyridineHCID 68510—
Reactant(2R)-3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acidHCID 2760712—
Reactant2-Bromo-4-phenylthioanilineHCID 22621282—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(R)-N-[2-Bromo-4-(phenylthio)phenyl]-2-hydroxy-2-methyl-3,3,3-trifluoropropanamideHCID 6911814130.1%

Reaction Steps

Oxalyl chloride (0.052 ml) was added to a stirred suspension of (R)-(+)-2-hydroxy-2-methyl-3,3,3-trifluoropropanoic acid (Method 9) (0.095 g) in dichloromethane (3 ml) containing DMF (1 drop). The mixture was stirred at ambient temperature for 2 hours and was then added to a solution of 2-bromo-4-phenylthioaniline (Method 17) (0.135 g) and 2,6-di-tert-butylpyridine (0.14 ml) in dichloromethane (5 ml) and stirred a further 3 hours. Volatile material was removed by evaporation and the residue was purified by chromatography on a silica gel Mega Bond Elut column eluting with 0-30% ethyl acetate/hexane to give the title compound (0.061 g) as a waxy solid. NMR: 1.59 (s, 3H), 7.25-7.50 (bm, 6H), 7.59 (s, 1H), 7.82 (bs, 1H), 7.98 (d,1H), 9.79 (s, 1H); MS: 420 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369273B1
Source datasetuspto-grants-2002_04
ORD IDord-7741708ff35043a1b71c1c5765b052fe
Source noteuspto-grants-2002_04