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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727493Generated: November 1, 2026

tert-Butanol → HCID 9989936, compound

https://huagongshe.com/reaction/727493

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantDiisopropylamineHCID 7912—
ReactantHexamethylphosphoramideHCID 12679—
Reactant2-Butene, 1-bromo-3-methyl-HCID 70092—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 9989936HCID 998993682%

Reaction Conditions

Temperature-75 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05712396
Source datasetuspto-grants-1998_01
ORD IDord-5b1d7155f4d5420cb4fd4743f0b998ba
Source noteuspto-grants-1998_01