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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043241Generated: November 1, 2026

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

https://huagongshe.com/reaction/1043241

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) in ether. After completion of the addition, the mixture was stirred at −78° C. for 2 hours and then 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, loaded onto an Analogix purification system, and eluted with 0-50% ethyl acetate in dichloromethane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557983B2
Source datasetuspto-grants-2013_10
ORD IDord-f5d8a7d568624fbebd096db55111f953
Source noteuspto-grants-2013_10