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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893225Generated: November 1, 2026

4-Phenylcyclohexanone → HCID 49763571, compound

https://huagongshe.com/reaction/1893225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PhenylcyclohexanoneHCID 78605—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86646678HCID 86646678—
SolventDichloromethaneHCID 6344—
ProductHCID 49763571HCID 49763571—

Reaction Steps

A solution of 4-phenyl-cyclohexanone (Aldrich, 1.5 g, 8.62 mmol) and N-(azetidin-3-ylcarbamoylmethyl)-3-trifluoromethyl-benzamide TFA salt (as prepared in the previous step, 3.89 g, 12.9 mmol) in DCM (20 mL) was treated with TEA (6 mL, 43 mmol) for 10 min followed by NaBH(OAc)3 (Aldrich, 3.65 g, 17.2 mmol) for another 4 hours at room temperature. The reaction was quenched with saturated sodium bicarbonate. The organic layer was separated and the aqueous layer was extracted 3 times with a chloroform/IPA “cocktail” (˜3:1, v/v). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated to give the crude product, which was then purified by a CombiFlash® system using ethyl acetate and 7N NH3 in MeOH as eluent (from pure ethyl acetate to 5% 7N NH3 in MeOH in ethyl acetate) to afford the two title compounds as white solids.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513229B2
Source datasetuspto-grants-2013_08
ORD IDord-b33e184be415416ab32c3477acd29bee
Source noteuspto-grants-2013_08