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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252039Generated: October 26, 2026

Dibromodifluoromethane → HCID 66889770, compound

https://huagongshe.com/reaction/252039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromodifluoromethaneHCID 6382—
Reactanttert-butyl N-methyl-N-(4-oxocyclohexyl)carbamateHCID 24820328—
CatalystZincHCID 23994—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66889770HCID 6688977060%

Reaction Steps

To a solution of methyl-(4-oxo-cyclohexyl)-carbamic acid tert-butyl ester (0.69 g, 3.04 mmol, 1.0 eq.) in THF (25 mL) at −30° C. was added CBr2F2 (1.25 mL, 4.5 eq.) followed slow addition of by P(N(CH3)2)3. The resulting mixture was warmed to room temperature over 0.5 h and Zn was introduced. The resulting mixture was stirred at reflux for 16 h, cooled to room temperature and diluted with Et2O. The organic phase was decanted and the aqueous phase extracted with 2×Et2O. The combined organic phase was washed with saturated CuSO4 solution until it stayed blue, dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography (20% EtOAc-Hexanes) to give (4-difluoromethylene-cyclohexyl)-methyl-carbamic acid tert-butyl ester (475 mg, 60%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868002B2
Source datasetuspto-grants-2011_01
ORD IDord-6128c433357048a9b921c3aea2790ce9
Source noteuspto-grants-2011_01