Water → Prostaglandin D2

HRID 436951

반응식

HRID 436951 반응식
[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][C@H:6]([OH:25])/[CH:7]=[CH:8]/[C@@H:9]1[C@@H:13]([CH2:14]/[CH:15]=[CH:16]\[CH2:17][CH2:18][CH2:19][C:20]([OH:22])=[O:21])[C@@H:12]([OH:23])[CH2:11][C@H:10]1[OH:24].CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.C(O)(C)C.O>CC(C)=O.C(OCC)C>[CH3:1][CH2:2][CH2:3][CH2:4][CH2:5][C@H:6]([OH:25])/[CH:7]=[CH:8]/[C@H:9]1[C:10](=[O:24])[CH2:11][C@H:12]([OH:23])[C@@H:13]1[CH2:14]/[CH:15]=[CH:16]\[CH2:17][CH2:18][CH2:19][C:20]([OH:22])=[O:21]

참가 물질

7

반응물 4

HCID 962WaterHCID 3776IsopropanolHCID 5280363DinoprostHCID 131709961Jones' reagent

생성물 1

HCID 448457Prostaglandin D2

시약·촉매·용매 2

HCID 180Acetone용매HCID 3283Diethyl Ether용매

반응 조건

온도
-40 °C

실험 절차

PGF2α, 15-(tetrahydropyranyl ether) (2 g.) in acetone (75 ml.) is cooled to -45° C. and thereafter treated with 1.2 ml. of the Jones reagent. The mixture is stirred for 30 min at -35 to -45° C. and thereafter treated with 0.5 ml. of isopropanol and stirred an additional 15 min. The reaction mixture is then poured into a mixture of ice, water, and diethyl ether. The mixture is then extracted with diethyl ether and the combined ethereal extracts washed with brine, and dried over sodium sulfate. After filtration removal of solvent proceeds by rotary evaporation . Crude product (1.8 g.) thereby obtained is chromatographed on 360 g. of silica gel eluting with 45 percent ethyl acetate in hexane. PGD2, 15-tetrahydropyranyl ether (800 mg.) is thereby obtained.

후처리

  1. additiontreated with 1.2 ml
  2. additiontreated with 0.5 ml
  3. extractionThe mixture is then extracted with diethyl ether
  4. washthe combined ethereal extracts washed with brine
  5. dry with materialdried over sodium sulfate
  6. filtrationAfter filtration removal of solvent proceeds
  7. customby rotary evaporation
  8. customCrude product (1.8 g.) thereby obtained
  9. customis chromatographed on 360 g

출처 및 근거

ORD 기록
ord-16a2c0ac3fb1423a96d011237866cdc6
출처 데이터셋
uspto-grants-1977_06
특허 번호
US04028419

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