반응 #531597

ord-f90f07a66ccb40a5a4e12733cb896cd1

반응 방정식

Cl
HCl
[Cl-].[NH4+]
NH4Cl
C#CCCO[Si](C)(C)C
Trimethylsilyl 3-butynyl ether
CCCCC.CCOCC
ether pentane
CSC
dimethyl sulfide
C=C(C)CCCC(=C)CCO
7-methyl-3-methylene-7-octen-1ol

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The resulting solution is cooled to -60°
  2. 2
    workup.ADDITIONanother 14 ml of dimethyl suflide is added
  3. 3
    workup.DISSOLUTIONto dissolve the precipitate that forms
  4. 4
    온도to warm to -25°
  5. 5
    workup.STIRRINGwith stirring for several hours
  6. 6
    workup.ADDITIONThe reaction is then poured into
  7. 7
    기타to warn to RT
  8. 8
    workup.STIRRINGstirred overnight
  9. 9
    추출The reaction is worked up by water and extraction with ether (2×)
  10. 10
    세척washed with sat (NH4)2SO4, water and brine
  11. 11
    여과filtered
  12. 12
    기타solvent removed

실험 절차

2.1 Grams (10.0 mmol) of the above complex is suspended in 15 ml of dry ether, and 12 ml of dimethyl sulfide is added under nitrogen. The resulting solution is cooled to -60° and another 14 ml of dimethyl suflide is added to dissolve the precipitate that forms. The Grignard reagent (24 ml, 9.6 mmol) from B above is added at -60° over 5 min and the reaction is stirred at -45° for 2 hr. Trimethylsilyl 3-butynyl ether (1.4 g, 9.8 mmol) (preparation follows) in ether/pentane (5 ml/30 ml) is added at -45°; the mixture is allowed to warm to -25° with stirring for several hours. The reaction is then poured into a pre-cooled (<-10°) solution of HCl/sat. NH4Cl, allowed to warn to RT and stirred overnight. The reaction is worked up by water and extraction with ether (2×). The ether phases are combined, washed with sat (NH4)2SO4, water and brine, filtered and solvent removed to give 7-methyl-3-methylene-7-octen-1ol.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04264518uspto-grants-1981_04