HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4,4,4-Trifluoro-2,2-dimethylbutan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ethyl 2,2-dimethyl-4,4,4-trifluorobutanoate | HCID 9990309 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4,4,4-Trifluoro-2,2-dimethylbutan-1-ol | HCID 59706997 | — |
Reaction Steps
To a solution of ethyl 4,4,4-trifluoro-2,2-dimethylbutanoate (1 g, 5.05 mmol) in ether (25 ml) under nitrogen was added LAH (1M solution in ether, 20.2 mmol) and allowed to stir at room temperature for one hour. Methanol was slowly added to R×n until bubbling stopped. The reaction was then suspended in ether and Water. The suspension was washed with Water, dried over sodium sulfate, filtered, and concentrated without heat to produce an oil 4,4,4-trifluoro-2,2-dimethylbutan-1-ol (75-1). 1H NMR (500 MHz, CDCl3) δ 3.4 (s, 2H), 2.20-2.01 (m, 2H), 1.05 (s, 6H). (M+H)+: observed=157.16, calculated=157.15
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765784B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-acc82fe7a09441d99dc41e8240c65117 |
| Source note | uspto-grants-2014_07 |