HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252039Generated: October 26, 2026
Dibromodifluoromethane → HCID 66889770, compound
https://huagongshe.com/reaction/252039
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibromodifluoromethane | HCID 6382 | — |
| Reactant | tert-butyl N-methyl-N-(4-oxocyclohexyl)carbamate | HCID 24820328 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66889770 | HCID 66889770 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868002B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-6128c433357048a9b921c3aea2790ce9 |
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| Source note | uspto-grants-2011_01 |
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