تفاعل #48668
ord-2df14d6ee4694d99b4c524f669c21778
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGStir for 1 hour at −78° C.
- 2أخرىSlowly quench the mixture with 0.1 N hydrochloric acid
- 3workup.ADDITIONDilute the resulting mixture with ethyl acetate
- 4workup.STIRRINGa saturated aqueous solution of sodium potassium tartrate (Rochelle salt) and stir the biphasic mixture overnight
- 5ترشيحFilter the mixture
- 6أخرىto remove
- 7أخرىprecipitates
- 8أخرىseparate the aqueous layer
- 9تركيزSaturate the aqueous phase with sodium chloride
- 10استخلاصextract with ethyl acetate
- 11workup.ADDITIONAdd the
- 12استخلاصorganic extract to the ethyl acetate solution of the reaction mixture
- 13غسيلwash the resultant mixture with saturated aqueous sodium chloride solution
- 14تجفيفdry (magnesium sulfate)
- 15ترشيحfilter
- 16تركيزconcentrate
الإجراء التجريبي
Cool lithium aluminum hydride (16 mL, 16 mmol, 1.0 M solution in tetrahydrofuran) under a nitrogen atmosphere to 0° C. Add tert-butanol (4.6 mL, 48.1 mmol) dropwise, warm to room temperature, and stir the resulting solution for 1 hour. Cool the hydride solution to −78° C. and add a solution of 3-tert-butylcyclobutanone (1 g, 7.9 mmol) in dry tetrahydrofuran (3 mL) dropwise. Stir for 1 hour at −78° C. and then warm to room temperature over 1 hour. Slowly quench the mixture with 0.1 N hydrochloric acid. Dilute the resulting mixture with ethyl acetate and a saturated aqueous solution of sodium potassium tartrate (Rochelle salt) and stir the biphasic mixture overnight. Filter the mixture to remove precipitates and separate the aqueous layer. Saturate the aqueous phase with sodium chloride and extract with ethyl acetate. Add the organic extract to the ethyl acetate solution of the reaction mixture and wash the resultant mixture with saturated aqueous sodium chloride solution, dry (magnesium sulfate), filter, and concentrate to give the title compound as a 9:1 mixture of cis/trans diastereomers.