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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254252Generated: November 2, 2026

(R)-Tert-butyl 3-(3-chlorobenzoyl)piperidine-1-carboxylate → 1,1-Dimethylethyl (3R)-3-[(1S)-1-(3-chlorophenyl)-5,5-difluoro-1-hydroxyhexyl]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1254252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-Tert-butyl 3-(3-chlorobenzoyl)piperidine-1-carboxylateHCID 46831638—
ReactantHCID 178461136HCID 178461136—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl (3R)-3-[(1S)-1-(3-chlorophenyl)-5,5-difluoro-1-hydroxyhexyl]-1-piperidinecarboxylateHCID 67191446—

Reaction Steps

A solution of (3R)-1-(tert-butoxycarbonyl)-3-(3-chlorobenzoyl)piperidine (100 mg, 0.33 mmol) in THF (2 mL) was cooled to −20° C. and 4,4-difluoropentylmagnesium chloride (˜0.79M in THF, 5.0 mL, 4.0 mmol) was added. The mixture was stirred for 2 h and quenched with sat'd NH4Cl. The aqueous layer was extracted with ether. The combined organic layers were washed with brine, dried over sodium sulfate and filtered. The solvent was removed on a roto-evaporator. The crude product was purified using flash chromatography (hexanes/EtOAc). N-Boc-(S)-1-(3-chlorophenyl)-5,5-difluoro-1-((R)-piperidin-3-yl)hexan-1-ol was isolated as an oil (70 mg) MS m/z 454 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455521B2
Source datasetuspto-grants-2013_06
ORD IDord-c7440de3710047f49472d579151c7426
Source noteuspto-grants-2013_06