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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432954Generated: October 26, 2026

Benzoyl chloride → n-Benzoyl-cis-4-hydroxy-d-proline methyl ester

https://huagongshe.com/reaction/432954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl (2R,4R)-4-hydroxypyrrolidine-2-carboxylate hydrochlorideHCID 12764090—
SolventDichloromethaneHCID 6344—
Productn-Benzoyl-cis-4-hydroxy-d-proline methyl esterHCID 147624890.7%

Reaction Steps

This ester was added in portions to a stirred mixture of 1500 mL of 1 N aqueous sodium bicarbonate and 500 mL of dichloromethane at 0-5° C., then 80 mL (97 g, 0.69 mol) of benzoyl chloride was added dropwise at 0-5° C., and the mixture was stirred at room temperature overnight. The phases were separated and the aqueous phase was extracted with dichloromethane (twice with 250 mL). The organic phases were combined, dried over magnesium sulfate, and evaporated under reduced pressure. The residue was triturated with toluene to afford 112.98 g (90.7% from cis4-hydroxy-D-proline) of N-benzoyl-cis-4-hydroxy-D-proline methyl ester as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664400B2
Source datasetuspto-grants-2003_12
ORD IDord-2292fd3a4d614286975d733427428fea
Source noteuspto-grants-2003_12