Aluminium lithium hydride → 4,4,4-Trifluoro-3-methylbut-2-en-1-ol

Temperature

0 °C

Benzyl 4,4,4-trifluoro-3-methylbut-2-enoate (1.87 g, 7.67 mmol) in diethyl ether (5 mL) was added dropwise to a suspension of LAH (291 mg, 1.67 mmol) in diethyl ether (10 mL). After stirring at −78° C. for 10 min and at 0° C. for a further 30 min, the reaction mixture was filtered through cotton, quenched with sodium potassium tartrate and stirred vigorously until layers separated. The aqueous phase was extracted with diethyl ether. The combined ethereal layers were dried (magnesium sulfate) and concentrated in vacuo to afford 4,4,4-trifluoro-3-methylbut-2-en-1-ol which was used in the subsequent step without further purification.

1. filtrationthe reaction mixture was filtered through cotton
2. customquenched with sodium potassium tartrate
3. stirringstirred vigorously until layers
4. customseparated
5. extractionThe aqueous phase was extracted with diethyl ether
6. dry with materialThe combined ethereal layers were dried (magnesium sulfate)
7. concentrationconcentrated in vacuo

ORD record

ord-b3e45da318d04b97a2bef486d048d6e7

Source dataset

uspto-grants-2012_06

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08193228B2