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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731490Generated: October 30, 2026

Cyclohexanone → HCID 178420523, compound

https://huagongshe.com/reaction/731490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantSodium AcetateHCID 517045—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 178511703HCID 178511703—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178420523HCID 178420523—

Reaction Steps

To a mixture of trans-4-phenoxycyclohexylamine (1 mmol) in 6 ml of THF and 6 ml of MeOH was added cyclohexanone (2 mmol), NaOAc (2 mmol) and 3 g of 3 Å molecular sieves. The mixture is stirred for 10 min after which 1N sodiumcyanoborohydride in tetrahydrofuran (2.4 mmol) is added. The reaction is stirred 1 day 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 crude cyclohexyl-(trans-4-phenoxy-cyclohexyl)amine which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582769B2
Source datasetuspto-grants-2009_09
ORD IDord-538ac8b7bd87498d9e9dddf310ad02f8
Source noteuspto-grants-2009_09