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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978306Generated: October 29, 2026

Methanol → tert-Butyl 4-(2-hydroxyethylidene)piperidine-1-carboxylate

https://huagongshe.com/reaction/1978306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactanttert-Butyl 4-(2-ethoxy-2-oxoethylidene)piperidine-1-carboxylateHCID 10333298—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantDiisobutylaluminumhydride tolueneHCID 86583787—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Producttert-Butyl 4-(2-hydroxyethylidene)piperidine-1-carboxylateHCID 22594495—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 19.901 g (73.888 mM) of tert-butyl 4-(ethoxycarbonylmethylene)piperidine-1-carboxylate in 100 ml of toluene was added 123 ml (185 mM) of 1.5 M diisobutylaluminum hydride-toluene at −78° C. and the mixture was stirred at −78° C. for 1 hour. Then, methanol was added at −78° C. and the mixture was stirred for 0.5 hour to decompose the excess diisobutylaluminum hydride. Then, water was added under ice-cooling and the mixture was stirred for 2 hours. The resulting precipitate was filtered off with the aid of celite and the celite was washed with ethyl acetate. The filtrate and washes were pooled and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=3/1 to 1/1) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-7a08bc61d12140b7927473d207b92021
Source noteuspto-grants-2001_05