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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631762Generated: October 26, 2026

Triethylamine → (2S)-1-oxo-1-(pyrrolidin-1-yl)propan-2-yl 2-bromo-2-(4-chlorophenyl)acetate

https://huagongshe.com/reaction/631762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(2S)-2-hydroxy-1-(1-pyrrolidinyl)-1-propanoneHCID 11051776—
ReactantBromo-4-chlorophenylacetyl chlorideHCID 12575778—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product(2S)-1-oxo-1-(pyrrolidin-1-yl)propan-2-yl 2-bromo-2-(4-chlorophenyl)acetateHCID 4264410759%

Reaction Steps

To a solution of (2S)-2-hydroxy-1-(pyrrolidin-1-yl)propan-1-one (24.0 g, 0.17 mol) in DCE (120 mL) was added triethylamine (84.69 g, 0.84 mol) and 2-bromo-2-(4-chlorophenyl)acetyl chloride (crude, 46.29 g, 0.17 mol) at 0° C. The reaction mixture was stirred for 2 h at RT. The reaction mixture was diluted with water (200 mL) and separated the organic layer. The organic layer was washed with 10% NaS2O3 (100 mL) and saturated sodium bicarbonate (60 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure. The crude residue was purified by flash column on 100-200 mesh silica-gel (20-25% ethyl acetate-hexane) to afford (2S)-1-oxo-1-(pyrrolidin-1-yl)propan-2-yl 2-bromo-2-(4-chlorophenyl)acetate 4 (37.5 g, 59%) as brown sticky gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321716B1
Source datasetuspto-grants-2016_04
ORD IDord-acf81ffc1af64838a48ecd215fbe61ec
Source noteuspto-grants-2016_04