HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 1,1,1-trifluoro-4-penten-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Ethanol, 1-ethoxy-2,2,2-trifluoro- | HCID 9897 | — |
| Reactant | Indium | HCID 5359967 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,1,1-trifluoro-4-penten-2-ol | HCID 10909642 | — |
Reaction Steps
To a suspension of indium powder (2.3 g, 20 mmol) in water is added allyl bromide (2.5 mL, 30 mmol) followed by trifluoroacetaldehyde ethyl hemiacetal (1.3 mL, 10 mmol). The reaction mixture is stirred for 16 h and then extracted with t-butyl methyl ether (50 mL). The organic layer is washed with water, brine, dried with Na2SO4 and concentrated to give the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700633B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-636cfc354b1d4693a020b3939d191a51 |
| Source note | uspto-grants-2010_04 |