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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184376Generated: October 30, 2026

Tert-butyl 3-oxopyrrolidine-1-carboxylate → tert-Butyl 3-hydroxy-3-methylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/2184376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl 3-hydroxy-3-methylpyrrolidine-1-carboxylateHCID 2295148537%

Reaction Steps

3-Oxo-pyrrolidine-1-carboxylic acid tert-butyl ester [Hofmann, J. Agric. Food Chem., 46, 3902 (1998)] (0.322 g, 1.74 mmol) was dissolved in diethyl ether (5 ml), cooled with an ice bath, and treated with methylmagnesium bromide (3M in ether, 0.64 ml, 1.91 mmol). The reaction was stirred for 1 h then more methylmagnesium bromide added, and the mixture stirred for 63 h. The reaction was quenched with aqueous ammonium chloride and extracted with diethyl ether (x3). The combined organic extracts were dried and evaporated. The residue was purified by flash chromatography, eluting with 0-50% ethyl acetate in petroleum ether, to give the title compound as a sticky off-white solid (0.129 g, 37%); NMR (CDCl3) 1.41 (3H, s), 1.46 (9H, s), 1.61 (1H, s), 1.79-1.92 (2H, m), and 3.17-3.58 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900345B2
Source datasetuspto-grants-2005_05
ORD IDord-3c9f871e193148fb9fe9861765b94596
Source noteuspto-grants-2005_05