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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346469Generated: October 30, 2026

tert-butyl (2S)-2-formylpyrrolidine-1-carboxylate → Tert-butyl (2S)-2-acetylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/346469

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (2S)-2-formylpyrrolidine-1-carboxylateHCID 2734674—
ReactantHCID 178418332HCID 178418332—
ProductTert-butyl (2S)-2-acetylpyrrolidine-1-carboxylateHCID 10465808—

Reaction Steps

25 ml (75 mmol) 3 M methylmagnesium chloride (diethyl ether) and 8.25 g (41.4 mmol) BOC-L-prolinal were allowed to react at −80° C. for 30 min according to procedure F. Yield of the crude product 9.19 g. The product was purified with a silica column using 33% ethyl acetate in petroleum ether as eluent. Yield 7.54 g (35.0 mmol 85%). The product was oxidized to the corresponding ketone according to procedure G. Yield of crude product 6.91 g. The product was purified with a silica column using 20–25% ethyl acetate in petroleum ether as eluent. Yield 5.61 g (26.3 mmol, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07173024B2
Source datasetuspto-grants-2007_02
ORD IDord-201f7ab94c124c3b8eee44a569b0fb0c
Source noteuspto-grants-2007_02