Methanol → 2-Benzoyloxy-4-hydroxymethylcyclobutanone

HRID 5959

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HRID 5959 반응식
[C:1]([O:9][CH:10]1[CH2:13][CH:12]([CH2:14][OH:15])[C:11]1=C)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)Cl.C[OH:21]>>[C:1]([O:9][CH:10]1[CH2:13][CH:12]([CH2:14][OH:15])[C:11]1=[O:21])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

4

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온도
-78 °C

실험 절차

A mixture of 2.09 g (9.5 mmol) of 1-benzoyloxy-3-hydroxymethyl-2-methylenecyclobutane from Step G, 112 mL of methylene chloride and 28 mL of methanol was cooled to -78° C. under a nitrogen atmosphere. Ozone was bubbled through the mixture for 10 minutes, until a persistent blue color was observed. Excess ozone was flushed out with nitrogen, 9 mL of dimethyl sulfide was added and the reaction mixture stirred for 0.5 h at -78° C. The reaction mixture was allowed to warm to ambient temperature, stirred for 0.5 h at ambient temperature and evaporated under reduced pressure to a syrup. The syrup (2.5 g) was dissolved to ~2 mL of methylene chloride and purified on a 1.5×45 cm silica gel column eluted @ 5 psi with 100 mL of methylene chloride, followed by 250 mL of 1% methanol in methylene chloride and 250 mL of 2% methanol in methylene chloride to give 1.79 g (86% yield) of the title compound; MS DCI-NH3M/Z: 221 (M+H)+, 238 (M+NH4)+.

후처리

  1. customOzone was bubbled through the mixture for 10 minutes, until a persistent blue color
  2. customExcess ozone was flushed out with nitrogen, 9 mL of dimethyl sulfide
  3. additionwas added
  4. temperatureto warm to ambient temperature
  5. stirringstirred for 0.5 h at ambient temperature
  6. customevaporated under reduced pressure to a syrup
  7. dissolutionThe syrup (2.5 g) was dissolved to ~2 mL of methylene chloride
  8. custompurified on a 1.5×45 cm silica gel column
  9. washeluted @ 5 psi with 100 mL of methylene chloride

출처 및 근거

ORD 기록
ord-399011f1b64c4ac8aa1d59f797b46087
출처 데이터셋
uspto-grants-1993_09
특허 번호
US05246931

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