tert-Butanol → HCID 9989936, compound

Temperature

-75 °C

To a stirred solution of 20.0 mL (142 mmol) of diisopropylamine in 160 mL of THF under argon at -10° C. was added a solution of 56 mL (140 mmol) of 2.5M n-butyllithium in hexane at a rate to keep the temperature below 0° C. The resulting light yellow solution was stirred 15 min and to this reaction mixture was added 20 mL (115 mmol) of HMPA. After an additional 10 min, the reaction was cooled to -75° C. and 18.8 mL (140 mmol) of 1,1-dimethylethanol, acetate ester was added at a rate to keep the temperature below -60° C. The resulting colorless solution was stirred for 30 min and 20 g (134 mmol) of 4-bromo-2-methyl-2-butene was added over 10 min. The reaction was stirred at -75° C. for 6 h and then warmed to room temperature. After 16, h, the reaction Was quenched with saturated ammonium chloride solution, extracted twice with ether, dried (MgSO4) and evaporated. Purification by distillation (b.p. 64°-67° C. @6 mmHg) gave title compound as a colorless oil, 20.1 g, 82% yield.

1. customthe temperature below 0° C
2. waitAfter an additional 10 min
3. customthe temperature below -60° C
4. stirringThe resulting colorless solution was stirred for 30 min
5. stirringThe reaction was stirred at -75° C. for 6 h
6. temperaturewarmed to room temperature
7. customAfter 16, h, the reaction Was quenched with saturated ammonium chloride solution
8. extractionextracted twice with ether
9. dry with materialdried (MgSO4)
10. customevaporated
11. customPurification
12. distillationby distillation (b.p. 64°-67° C. @6 mmHg)

ORD record

ord-964dcd66454a4447be5f79a7dc717d98

Source dataset

uspto-grants-1996_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05567841