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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666430Generated: October 30, 2026

Carbon tetrabromide → Tert-butyl 4-(dibromomethylene)piperidine-1-carboxylate

https://huagongshe.com/reaction/1666430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(dibromomethylene)piperidine-1-carboxylateHCID 53486134120.2%

Reaction Steps

To a stirred solution of triphenylphosphine (155.6 g, 0.59 mol) in dry dichloromethane (870 mL) at 0° C. was added carbon tetrabromide (100.86 g, 0.304 mol) portionwise. The mixture was stirred at RT for 30 min and then cooled to −78° C. A solution of tert-butyl 4-oxopiperidine-1-carboxylate (30 g, 0.15 mol) in CH2Cl2 (90 mL) was added dropwise and the reaction was stirred at −78° C. for 30 min and then at RT overnight. The mixture was filtered and the filtrate was evaporated to dryness. Diethyl ether was added and the mixture was filtered again. The filtrate was evaporated to dryness to give the title compound (64 g). 1H NMR (500 MHz, CDCl3): δ 3.44 (m, 4H), 2.46 (m, 4H), 1.47 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044052B2
Source datasetuspto-grants-2011_10
ORD IDord-9bc8205664f945a08a7b88b5373d47c6
Source noteuspto-grants-2011_10