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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532773Generated: October 30, 2026

1-Chloroethyl chloroformate → (3S,4R)-methyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate

https://huagongshe.com/reaction/532773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant(3S,4R)-methyl 1-benzyl-4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylateHCID 66617857—
Solvent1,2-DichloroethaneHCID 11—
Product(3S,4R)-methyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylateHCID 5144121998.3%

Reaction Steps

1-Chloroethyl chloroformate (1.5 mL, 13.9 mmol) was added to a solution of (3S,4R)-methyl 1-benzyl-4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate (4.20 g, 11.5 mmol) in DCE (50 mL) at 0° C. The mixture was refluxed for 1 hour. After cooling, the solvent was removed under vacuum at 65° C. for 1 hour. MeOH (50 mL) was added to the residue and refluxed for 1 hour. The MeOH was removed. The solid was redissolved in CHCl3 and treated with saturated Na2CO3. The aqueous layer was separated and extracted with CHCl3 (2×30 mL). The organic phase was combined and dried. The solvent was removed to afford (3S,4R)-methyl 4-(3,4-dichlorophenyl)pyrrolidine-3-carboxylate (3.1 g, 98%). (LCMS (APCI+) [M+H]+ 274.1; Rt: 2.25 min.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853199B2
Source datasetuspto-grants-2014_10
ORD IDord-3a7ceadfe6634dc3be3a55d76a571edc
Source noteuspto-grants-2014_10