Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848057Generated: November 1, 2026

Sodium Hydroxide → (1-(Aminomethyl)cyclohexyl)methanol

https://huagongshe.com/reaction/1848057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantMethyl 1-cyanocyclohexane-1-carboxylateHCID 11182833—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product(1-(Aminomethyl)cyclohexyl)methanolHCID 2237948658.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of methyl 1-cyanocyclohexanecarboxylate (2 g, 11.96 mmol) in anhydrous THF (40 mL) at rt was added portionwise LiAlH4 (1.36 g, 35.88 mmol). The reaction vessel was sealed and the mixture was heated at 80° C. for 5 h. The mixture was cooled to 0° C. and water (1 mL), 1M aq NaOH (1 mL), and water (3 mL) were added sequentially. To the resulting mixture were added DCM and saturated aq sodium potassium tartrate, and the mixture was stirred for 3 h. The organic layer was separated and further washed with brine. The organic layer was separated, dried over MgSO4, filtered, and concentrated under reduced pressure to afford (1-(aminomethyl)cyclohexyl)methanol (1 g) which was not purified further. LCMS (ESI) m/z 144 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952058B2
Source datasetuspto-grants-2015_02
ORD IDord-40ab976a1e3a4bc590e572b67738b5a9
Source noteuspto-grants-2015_02