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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520720Generated: November 4, 2026

4-(Aminomethyl)cyclohexanone, N-BOC protected → HCID 86647903, compound

https://huagongshe.com/reaction/1520720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)cyclohexanone, N-BOC protectedHCID 40424027—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86647903HCID 86647903—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of tert-butyl (4-oxocyclohexyl)methylcarbamate (1.00 g) was dissolved in tetrahydrofuran (20 mL) and cooled to −78° C. Methylmagnesium bromide (4.40 mL) was added dropwise. The reaction was stirred for 2 hours at −78° C. then allowed to warm to 0° C. and stirred for 30 minutes. The resulting suspension was quenched with water (10 mL), diluted with ether (50 mL) and washed with ammonium chloride (25 mL) and brine (25 mL), dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography (Reveleris 80 g) eluting using a gradient of 5% to 50% ethyl acetate/dichloromethane over 30 minutes (flow=60 ml/min) gave the title compound as a ˜2:1 mixture of cis and trans isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073855B2
Source datasetuspto-grants-2015_07
ORD IDord-283d9303446046a596d2baf50e5e472d
Source noteuspto-grants-2015_07