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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777354Generated: November 4, 2026

Carbon tetrabromide → Ethyl 4-(3-bromopropyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/1777354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant1-Tert-butyl 4-ethyl 4-(3-hydroxypropyl)piperidine-1,4-dicarboxylateHCID 57815239—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(3-bromopropyl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylateHCID 67539218—

Reaction Steps

Carbon tetrabromide (1.6 gm, 0.0048 mol) is added to a stirred solution of 4-(3-hydroxypropyl) piperidine-1,4-dicarboxylic acid-1-tert-butyl ester-4-ethyl ester (1.27 gm, 0.0040 mol) and triphenyl phosphine (1.6 gm, 0.0060 mol) in dichloromethane (15 mL) at 0-5° C. temperature. Reaction mixture is allowed to stir at room temperature for 30 minutes. Removal of solvent gives a crude residue which is purified by column chromatography (silica gel 230-400 mesh, ethyl acetate:n-hexane 3:7) to get 4-(3-bromopropyl)piperidine-1,4-dicarboxylic acid-1-tert-butyl ester-4-ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266867B2
Source datasetuspto-grants-2016_02
ORD IDord-70e5d75e610f49728e35a6b0da7832f8
Source noteuspto-grants-2016_02