تفاعل #44493

ord-cacae96a195b4eb7a82169604af3d677

معادلة التفاعل

[H-].[Na+]
NaH
OCC=CCO
but-2-ene-1,4-diol
CC(C)(C)[Si](Cl)(c1ccccc1)c1ccccc1
tert-butyl-chlorodiphenylsilane
CC(C)(C)[Si](OCC=CCO)(c1ccccc1)c1ccccc1
4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.STIRRINGstirred for another two hours
  3. 3
    workup.ADDITIONwas added drop wise
  4. 4
    workup.WAITAfter twenty minutes
  5. 5
    أخرىthe cooling bath was removed
  6. 6
    workup.STIRRINGto stir overnight at room temperature
  7. 7
    workup.ADDITIONSaturated NH4Cl was poured into the reaction mixture
  8. 8
    أخرىthe reaction was partitioned with diethyl ether (200 mL)
  9. 9
    غسيلThe organic layer was washed with brine
  10. 10
    تجفيفdried (MgSO4)
  11. 11
    ترشيحfiltered
  12. 12
    أخرىThe resulting oil was used in the following step without further purification

الإجراء التجريبي

NaH (3 g, 75 mmol, 60% in oil) was added portion-wise to a stirred and cooled (0° C.) solution of but-2-ene-1,4-diol (6 g, 68.09 mmol) in dry tetrahydrofuran (250 mL). After the addition, the mixture was allowed to warm to room temperature and stirred for another two hours. The resulting white mixture was then cooled (0° C.) and tert-butyl-chlorodiphenylsilane (15.7 mL, 61.28 mmol) was added drop wise. After twenty minutes, the cooling bath was removed and the mixture was allowed to stir overnight at room temperature. Saturated NH4Cl was poured into the reaction mixture and the reaction was partitioned with diethyl ether (200 mL). The organic layer was washed with brine, dried (MgSO4), and filtered. The resulting oil was used in the following step without further purification.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07737137B2uspto-grants-2010_06