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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361872Generated: October 30, 2026

Dibromodifluoromethane → HCID 11608680, compound

https://huagongshe.com/reaction/2361872

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 numberUS08691814B2
Source datasetuspto-grants-2014_04
ORD IDord-5c694713c7274ef1bdf394590745fc61
Source noteuspto-grants-2014_04