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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242546Generated: October 28, 2026

Tert-butyl 3-oxopyrrolidine-1-carboxylate → HCID 18675808, compound

https://huagongshe.com/reaction/242546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18675808HCID 1867580860%

Reaction Steps

To a stirred solution of 1-t-butoxycarbonyl-3-pyrrolidinone (0.57 g, 3.23 mmol) in THF (10 mL) was added 4-chlorophenyl magnesium bromide (1.0 M, 5.2 mL) under the protection of argon at 0° C. The reaction was stirred at room temperature for 1 hour then quenched by the addition of saturated aqueous NH4OH (8 mL). The aqueous layer was extracted with EtOAc (50 mL×2), dried over MgSO4 and concentrated in vacuo. Chromatographic purification on silica gel (Hexane/EtOAc=3/1) provided 0.57 g 1-t-butoxycarbonyl-3-(4-chlorophenyl)-3-hydroxypyrrolidine (60%). m/z 298 (m+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-09ded3fd6f6147688b8563e750d9178c
Source noteuspto-grants-2014_02