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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500066Generated: October 25, 2026

Cerium(III) chloride → tert-butyl N-(4-butyl-4-hydroxycyclohexyl)carbamate

https://huagongshe.com/reaction/500066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCerium(III) chlorideHCID 24636—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Producttert-butyl N-(4-butyl-4-hydroxycyclohexyl)carbamateHCID 68459705—

Reaction Steps

Under nitrogen atmosphere, anhydrous cerium chloride (4.63 g) was added to anhydrous tetrahydrofuran (50 ml), and the mixture was stirred at room temperature for 2 hours. After the suspension was cooled to −78° C., 1.6 M butyl lithium in hexane (6.40 ml) was added to the suspension and then the mixture was stirred for 1 hour. A solution of t-butyl 4-oxocyclohexylcarbamate (2.36 g) in anhydrous tetrahydrofuran (50 ml) was added to the reaction mixture over 10 minutes, and the mixture was gradually warmed to about 25° C. and then stirred overnight. After a saturated aqueous ammonium chloride was added to the reaction mixture, the mixture was filtrated through Celite. The filtrate was extracted with ethyl acetate, and the organic layer was washed with brine, dried over sodium sulfate, and the solvent was removed in vacuo. The residue was purified by a silica gel chromatography (eluent: chloroform/methanol=100/1) to give 2.53 g of t-butyl 4-butyl-4-hydroxycyclohexylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767854B2
Source datasetuspto-grants-2010_08
ORD IDord-4396b45a7eaf410bb1da4ae72f8315c5
Source noteuspto-grants-2010_08