반응 #48663

ord-3c8048ba8345462682c89c2f674e7eb4

반응 방정식

O=C1CCOCC1
tetrahydropyran-4-one
N#CCCl
chloroacetonitrile
CC(C)(C)[O-].[K+]
potassium tert-butoxide
N#CC1OC12CCOCC2
desired compound
수율 59.1%
N#CC1OC12CCOCC2
1,6-Dioxa-spiro[2,5]octane-2-carbonitrile
수율 59.1%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONadd
  2. 2
    기타over 20 minutes
  3. 3
    기타quench slowly with 1 N hydrochloric acid
  4. 4
    추출Extract with diethyl ether (×3)
  5. 5
    세척Combine extracts and wash with saturated aqueous sodium chloride solution
  6. 6
    건조dry (magnesium sulfate)
  7. 7
    여과filter
  8. 8
    농축concentrate
  9. 9
    기타purify
  10. 10
    세척(silica gel chromatography, eluting with 0:100 to 1:1 ethyl acetate:hexanes)

실험 절차

Dissolve tetrahydropyran-4-one (5.0 mL, 54.2 mmol) and chloroacetonitrile (3.4 mL, 53.5 mmol) in tert-butanol (1 mL) and add drop-wise a solution of potassium tert-butoxide (54 mL, 54 mmol, 1.0 M in tert-butanol) over 20 minutes. Stir for 16 hours, dilute with water and quench slowly with 1 N hydrochloric acid. Extract with diethyl ether (×3). Combine extracts and wash with saturated aqueous sodium chloride solution, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 0:100 to 1:1 ethyl acetate:hexanes) to give the desired compound as a light yellow oil (4.4 g, 59%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745438B2uspto-grants-2010_06