HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl trifluoromethyl ketone → Benzyl 4,4,4-trifluoro-3-methylbut-2-enoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl trifluoromethyl ketone | HCID 9871 | — |
| Reactant | Benzyl 2-(triphenyl-lambda5-phosphanylidene)acetate | HCID 3862746 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 4,4,4-trifluoro-3-methylbut-2-enoate | HCID 66705445 | — |
Reaction Steps
1,1,1-Trifluoroacetone (680 mg, 6.1 mmol) was added to an ambient temperature solution of benzyl (triphenylphosphoranylidene)acetate (2.5 g, 6.1 mmol) in methylene chloride (10 mL). After stirring in a sealed tube for 72 h, the reaction mixture was concentrated in vacuo. Chromatography over silica eluting with 0-20% ethyl acetate/hexane afforded benzyl 4,4,4-trifluoro-3-methylbut-2-enoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08193228B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-787f6bbc5f2b4757878113bd726cbc64 |
| Source note | uspto-grants-2012_06 |