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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249884Generated: October 30, 2026

Dibromodifluoromethane → HCID 11608680, compound

https://huagongshe.com/reaction/2249884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromodifluoromethaneHCID 6382—
ReactantHexamethylphosphoramideHCID 12679—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11608680HCID 1160868056%

Reaction Steps

To a solution of 4-oxo-piperidine-1-carboxylic acid benzyl ester (0.50 g, 2.14 mmol, 1.0 eq.) in THF (20 mL) was added dibromodifluoromethane (0.90 mL, 4.5 eq.) at −30° C. followed by HMPA (1.75 mL, 4.5 eq.). The cooling bath was removed and the reaction mixture was swirled periodically. After 30 min, zinc dust (0.63 g, 4.5 eq.) and HMPA (80 μL 0.4 eq.) was added and the mixture was heated at reflux for 18 h. Upon cooling to room temperature, the residue was washed with diethyl ether several times. The combined ether washings were washed successively with saturated aqueous copper (II) sulphate, brine, dried over Na2SO4 and concentrated. The residue was purification by chromatography (20% EtOAc-hexanes) to afford 4-difluoromethylene-piperidine-1-carboxylic acid benzyl ester (0.32 g, 56%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314936B2
Source datasetuspto-grants-2008_01
ORD IDord-34b0c99d40814169ac17e2f972e485b3
Source noteuspto-grants-2008_01