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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457035Generated: October 30, 2026

Acetic Acid → HCID 66758909, compound

https://huagongshe.com/reaction/457035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86585734HCID 86585734—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 66758909HCID 6675890969.8%

Reaction Steps

To a solution of the product of step 1 (90 mg) in dichloromethane (6 ml) were added sodium triacetoxyborohydride (170 mg), 4-(4-chlorophenyl)-4-hydroxypiperidine (70 mg) and acetic acid (0.02 ml) and the mixture stirred at room temperature for 24 hour. Water and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography eluting with dichloromethane-methanol (95:5) to give 4-(4-chlorophenyl)-1-[4-(5,11-dihydro-7-methoxy[1]benzoxepino[2,3-b]pyridin-5-ylidene)buten-2-yl]piperidin-4-ol (110 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186729B2
Source datasetuspto-grants-2007_03
ORD IDord-7bb4a65664a64e5b93c577af6d429939
Source noteuspto-grants-2007_03