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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864000Generated: November 1, 2026

Cyclohexane → (S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1864000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexaneHCID 8078—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylateHCID 1514448—
SolventDichloromethaneHCID 6344—
Product(S)-tert-Butyl 3-(bromomethyl)piperidine-1-carboxylateHCID 3417703591%

Reaction Steps

To a solution of 1,1-dimethylethyl (3S)-3-(hydroxymethyl)-1-piperidinecarboxylate (30.0 g, 139 mmol) and carbon tetrabromide (72.0 g, 217 mmol) in methylene chloride (150 mL) was added dropwise a solution of triphenyl phosphine (42.4 g, 162 mmol) in methylene chloride (150 mL). An ice-bath was used to maintain an internal temperature between 20 and 25° C. during the addition. After stirring the mixture at ambient temperature for 1 h, cyclohexane (500 mL) was added. Approximately one-half of the solvent was removed under reduced pressure. The remaining solution was cooled in an ice bath and the resulting precipitate was removed by filtration. The filtrate was concentrated under reduced pressure and the residue subjected to flash chromatography (0% to 25% ethyl acetate/hexanes, silica gel) to give 35.1 g (91% yield) of the desired product as a solid. MS (ES+) m/z 278 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625890B2
Source datasetuspto-grants-2009_12
ORD IDord-6649e41ae8554d88b45db195e9a9556a
Source noteuspto-grants-2009_12