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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060236Generated: November 2, 2026

Ethyl chloroformate → 1-(4-Methoxy-benzoyl)-pyrrolidine-3,3-dicarboxylic acid diethyl ester

https://huagongshe.com/reaction/2060236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(4-Methoxy-benzoyl)-pyrrolidine-3-carboxylic acid ethyl esterHCID 59322175—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Methoxy-benzoyl)-pyrrolidine-3,3-dicarboxylic acid diethyl esterHCID 5932222794%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Lithium bis(trimethylsilyl)amide (1000 mL of a 1.0M solution in tetrahydrofuran, 1.0 mol) was added to a stirred solution of 1-(4-methoxy-benzoyl)-pyrrolidine-3-carboxylic acid ethyl ester (±) (268 g, 0.97 mol) (see Preparation 2) in THF (1600 mL) at −70° C. The mixture was stirred for 20 mins at −70° C. then ethyl chloroformate (104 mL, 1.09 mol) was added over 15 minutes. The resulting mixture was stirred at −60° C. for 1 hour. The reaction mixture was quenched with 10% citric acid aqueous solution (1200 mL) at −50° C. then warmed to room temperature. The organic layer was separated, washed with saturated aqueous NaHCO3 (1200 mL) and water (1200 mL) then concentrated under reduced pressure to afford the title compound as an orange oil (316.0 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278343B2
Source datasetuspto-grants-2012_10
ORD IDord-4522435021274fd3a1cbd5ed93c1147b
Source noteuspto-grants-2012_10