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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57622Generated: October 29, 2026

Sodium borohydride → (S)-tert-butyl 3-(1-hydroxyethyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/57622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl (3S)-3-acetylpyrrolidine-1-carboxylateHCID 68071565—
SolventMethanolHCID 887—
Product(S)-tert-butyl 3-(1-hydroxyethyl)pyrrolidine-1-carboxylateHCID 71113442—

Reaction Steps

To a solution of (S)-tert-butyl 3-acetylpyrrolidine-1-carboxylate in methanol (10 mL) was added sodium borohydride (114 mg, 3.0 mmol) at 0° C. The reaction mixture was stirred at ambient temperature for 2 hours then quenched with saturated ammonium chloride solution and extracted with dichloromethane. The combined extracts were dried over magnesium sulfate, filtered, and concentrated to give the title compound for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-4fb5d22d6b59418ba567344c09e3fb35
Source noteuspto-grants-2016_09