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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040306Generated: October 30, 2026

Benzyl [(4-oxocyclohexyl)methyl]carbamate → HCID 86647915, compound

https://huagongshe.com/reaction/2040306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl [(4-oxocyclohexyl)methyl]carbamateHCID 50999237—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86647915HCID 86647915—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a vigorous stirring solution of benzyl (4-oxocyclohexyl)methylcarbamate (1 g) in tetrahydrofuran (20 mL) at −78° C. was slowly added 1 M ethylmagnesium bromide (11.48 ml, 11.48 mmol) in ether. After completion of the addition, the mixture was stirred at −78° C. for 2 hours and was warmed to 0° C., and stirred in an ice bath for 30 minutes. The reaction was quenched with a cold NH4Cl aqueous solution. The precipitates were filtered off and washed with ethyl acetate. The filtrate was concentrated. The residue was dissolved in dichloromethane and loaded onto Analogix purification system, and was eluted with 0-50% ethyl acetate in dichloromethane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580794B2
Source datasetuspto-grants-2013_11
ORD IDord-85d486706e9d474f9fde5287a325bb85
Source noteuspto-grants-2013_11