HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylcyclohexanone → 4-tert-butyl-1,1-difluorocyclohexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylcyclohexanone | HCID 7392 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 4-Fluoroanisole | HCID 9987 | — |
| Reactant | N-ethyl-N-phenylaminosulfur trifluoride | HCID 20650010 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-tert-butyl-1,1-difluorocyclohexane | HCID 640499 | 99% |
Reaction Steps
A solution of 4-t-butylcyclohexanone (308 mg, 2.0 mmol) in CH2Cl2 (10.0 mL) was added to N-ethyl-N-phenylaminosulfur trifluoride (627 mg, 3.0 mmol ) at room temperature under N2. BF3.OEt2 (100 mL) was added and the mixture was stirred for 6 h at room temperature. The mixture was washed with saturated NaHCO3, dried (Na2SO4), filtered and evaporated in vacuo. Proton and Fluorine NMR with 4-fluoroanisole (2 mmol) as internal standard showed that a 99% yield of 1,1-difluoro-4-t-butylcyclohexane was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06222064B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-edf018d1ba4442aaa2d395a1591c8bd7 |
| Source note | uspto-grants-2001_04 |