تفاعل #48668

ord-2df14d6ee4694d99b4c524f669c21778

معادلة التفاعل

[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
CC(C)(C)O
tert-butanol
CC(C)(C)C1CC(=O)C1
3-tert-butylcyclobutanone
[H-]
hydride
CC(C)(C)[C@H]1C[C@@H](O)C1
title compound
CC(C)(C)[C@H]1C[C@@H](O)C1
Cis-3-tert-butylcyclobutanol

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGStir for 1 hour at −78° C.
  2. 2
    أخرىSlowly quench the mixture with 0.1 N hydrochloric acid
  3. 3
    workup.ADDITIONDilute the resulting mixture with ethyl acetate
  4. 4
    workup.STIRRINGa saturated aqueous solution of sodium potassium tartrate (Rochelle salt) and stir the biphasic mixture overnight
  5. 5
    ترشيحFilter the mixture
  6. 6
    أخرىto remove
  7. 7
    أخرىprecipitates
  8. 8
    أخرىseparate the aqueous layer
  9. 9
    تركيزSaturate the aqueous phase with sodium chloride
  10. 10
    استخلاصextract with ethyl acetate
  11. 11
    workup.ADDITIONAdd the
  12. 12
    استخلاصorganic extract to the ethyl acetate solution of the reaction mixture
  13. 13
    غسيلwash the resultant mixture with saturated aqueous sodium chloride solution
  14. 14
    تجفيفdry (magnesium sulfate)
  15. 15
    ترشيحfilter
  16. 16
    تركيزconcentrate

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745438B2uspto-grants-2010_06