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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928104Generated: October 31, 2026

HCID 178418573, compound → HCID 178468180, compound

https://huagongshe.com/reaction/928104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418573HCID 178418573—
ReactantHCID 178502729HCID 178502729—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178468180HCID 178468180—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of benzyl {trans-4-[methoxy(methyl)carbamoyl]cyclohexyl}carbamate (3.43 g, 10.71 mmol) in THF (107 mL) at 0° C. was added methylmagnesium bromide (3.0 M in diethyl ether, 5.35 mL, 16.06 mmol) and the reaction was stirred for one hour at 0° C. An additional portion of methylmagnesium bromide (3.0 M in diethyl ether, 5.35 mL, 16.06 mmol) was then added and the reaction was allowed to warm to room temperature and then stirred for one hour. The reaction was slowly quenched with aqueous saturated ammonium chloride. Water and ethyl acetate were added and the organic layer was separated, dried over magnesium sulfate, filtered and concentrated to afford benzyl (trans-4-acetylcyclohexyl)carbamate that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290490B2
Source datasetuspto-grants-2016_03
ORD IDord-e6cd24a2b35c4a7b9689aeae7d4b3503
Source noteuspto-grants-2016_03