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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731465Generated: October 30, 2026

Cyclohexanone → HCID 178420520, compound

https://huagongshe.com/reaction/731465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178511557HCID 178511557—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178420520HCID 17842052087.5%

Reaction Steps

Trans-4-phenoxymethylcyclohexylamine trifluoroacetate (1.2 mmol) is dissolved in a mixture of 4 ml of THF and 4 mL of MeOH in a 20 ml glass vial equipped with a magnetic stirrer and a screw cap. 117 mg of cyclohexanone and 3 g of 3 Å molecular sieves are added. The mixture is stirred for 10 min. after which 2.4 mL of 1N sodiumcyanoborohydride in tetrahydrofuran is added. The reaction stirred 4 days at room temperature then filtered through celite washing through with 30 mL of dichloromethane. The organic phase is washed with 10 mL of water, 10 mL of brine, dried (MgSO4), filtered and concentrated in vacuo to give 300 mg of cyclohexyl-(trans-4-phenoxymethyl-cyclohexyl)-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582769B2
Source datasetuspto-grants-2009_09
ORD IDord-73de901e6a394524869af492cd8e1c84
Source noteuspto-grants-2009_09