Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516209Generated: October 30, 2026

Hydrochloric Acid → (S)-Phenyl(1-(3-chloro-2,6-difluorophenyl)-3-oxopropyl)carbamate

https://huagongshe.com/reaction/516209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhenyl chloroformateHCID 15891—
Reactant(S)-Phenyl(1-(3-chloro-2,6-difluorophenyl)but-3-en-1-yl)carbamateHCID 131733335—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(S)-Phenyl(1-(3-chloro-2,6-difluorophenyl)-3-oxopropyl)carbamateHCID 8940838340%

Reaction Steps

(S)-Phenyl(1-(3-chloro-2,6-difluorophenyl)but-3-en-1-yl)carbamate: To a solution of crude Intermediate 17B (1.17 g, 3.64 mmol) in MeOH (10 mL) was added HCl (5 mL, 20.00 mmol) and the reaction was stirred at rt for 1 h. After 1 h, the reaction mixture was concentrated and dried under vacuum to obtain a pale yellow solid. The solid was dissolved in ACN (25 mL) followed by addition of TEA (1.520 mL, 10.91 mmol). The above reaction mixture was cooled to 0° C. To this mixture was added phenyl chloroformate (0.502 mL, 4.00 mmol) dropwise and the resulting reaction was stirred at 0° C. for 1 h. The reaction mixture was then diluted with EtOAc and washed with water followed by brine. The crude product was then purified by silica gel chromatography to give the desired product (490 mg, 40%) as clear oil. MS (ESI) m/z: 338.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108981B2
Source datasetuspto-grants-2015_08
ORD IDord-75fae04c41dd4972912e121f1787796b
Source noteuspto-grants-2015_08