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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066819Generated: November 1, 2026

Sodium borohydride → 4-(t-butoxycarbonylamino)-2,2-dimethylbutanol

https://huagongshe.com/reaction/1066819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1,1-Dimethylethyl 3,3-dimethyl-2-oxo-1-pyrrolidinecarboxylateHCID 10856825—
SolventEthanolHCID 702—
Product4-(t-butoxycarbonylamino)-2,2-dimethylbutanolHCID 1096596993%

Reaction Steps

A solution of 3,3-dimethyl-1-(t-butoxycarbonyl)pyrrolidin-2-one (3.35 g, 15.7 mmol) in absolute ethanol under a nitrogen atmosphere was treated with sodium borohydride (1.79 g, 47.1 mmol). The resulting mixture was stirred at ambient tempeature for about 24 hours. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with sodium bicarbonate. The aqueous fraction was back extracted twice with ethyl acetate. The organic phase was dried over sodium sulfate and concentrated in vacuo. The residue was further purified by chromatography to yield 3.17 grams (93%) of the title intermediate as a clear oil. mp 75.5-76.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245761B1
Source datasetuspto-grants-2001_06
ORD IDord-8b6714537f524cac84c8047478e1eacb
Source noteuspto-grants-2001_06