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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79885Generated: October 25, 2026

Benzyl chloroformate → O1-benzyl O2-methyl 4-methylenepyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/79885

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant1-(tert-Butoxycarbonyl)-4-methylenepyrrolidine-2-carboxylic acidHCID 21762564—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductO1-benzyl O2-methyl 4-methylenepyrrolidine-1,2-dicarboxylateHCID 2192264756%

Reaction Steps

4-Methylene-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (12.00 g, 52.80 mmol) was dissolved in MeOH (200 mL) and treated with 4.0 M HCl/dioxane (50 mL). After stirring for 3.5 hours at room temperature, the reaction mixture was concentrated under reduced pressure. The crude residue was dissolved in DCM (200 mL) and treated with DIPEA (22 mL, 127 mmol) and BnOCOCl (9.64 mL, 63.4 mmol). After stirring for 1 hours at room temperature, the reaction mixture was poured into H2O. The aqueous layer was extracted 3× with DCM. The combined organics were dried over MgSO4, filtered and concentrated. The residue was purified by silica column chromatography (10% to 25% EtOAc/hexane) to provide 4-Methylene-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester 2-methyl ester (8.20 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841278B2
Source datasetuspto-grants-2014_09
ORD IDord-a91308c89c7240a28b622a00cc69d337
Source noteuspto-grants-2014_09