HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexafluoroacetone → 1,1,1-Trifluoro-2-trifluoromethyl-but-3-yn-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexafluoroacetone | HCID 12695 | — |
| Reactant | HCID 178418486 | HCID 178418486 | — |
| Product | 1,1,1-Trifluoro-2-trifluoromethyl-but-3-yn-2-ol | HCID 13667828 | — |
Reaction Steps
To a 100 ml solution of ethynyl magnesium bromide (0.5 M in THF) in an acetone-ethanol dry ice bath was bubbled hexafluoro acetone gas (6.1 g, 36.7 mmol) over 2 h. The reaction mixture was warmed to r.t and then refluxed for 0.5 h. The reaction mixture was quenched with aqueous NH4Cl solution and extracted with ether. The combined organic phases were washed with brine, and dried over MgSO4. A liquid mixture of 1,1,1-trifluoro-2-trifluoromethyl-but-3-yn-2-ol with THF at b.p. 100-103° C. (4.7 g, contained about 68 mol % THF) was obtained by distillation (12 inch Vigreux column).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524969B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-bc101de70dbe4fdab6d0c8d48c1a3cbf |
| Source note | uspto-grants-2009_04 |