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p-Toluenesulfonic acid → 7alpha-(5-Acetoxypentyl)-3,17beta-bis-(tetrahydropyran-2-yloxy)-estra-1,3,5(10)-triene

HRID 1595969
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HRID 1595969 반응식
[C:1]([O:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C@@H:10]1[CH2:27][C:26]2[CH:25]=[C:24]([OH:28])[CH:23]=[CH:22][C:21]=2[C@@H:20]2[C@@H:11]1[C@H:12]1[C@@:16]([CH2:18][CH2:19]2)([CH3:17])[C@@H:15]([OH:29])[CH2:14][CH2:13]1)(=[O:3])[CH3:2].[O:30]1[CH:35]=[CH:34][CH2:33][CH2:32][CH2:31]1.[C:36]1(C)C=[CH:40][C:39](S(O)(=O)=O)=[CH:38][CH:37]=1.C(=O)(O)[O-:48].[Na+]>O1CCCC1.C(OCC)(=O)C>[C:1]([O:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][C@@H:10]1[CH2:27][C:26]2[CH:25]=[C:24]([O:28][CH:35]3[CH2:34][CH2:33][CH2:32][CH2:31][O:30]3)[CH:23]=[CH:22][C:21]=2[C@@H:20]2[C@@H:11]1[C@H:12]1[C@@:16]([CH2:18][CH2:19]2)([CH3:17])[C@@H:15]([O:29][CH:40]2[CH2:39][CH2:38][CH2:37][CH2:36][O:48]2)[CH2:14][CH2:13]1)(=[O:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 6101p-Toluenesulfonic acidHCID 80803,4-dihydro-2H-pyranHCID 516892Sodium BicarbonateHCID 70191893HCID 70191893, 화합물

생성물 1

HCID 206838777alpha-(5-Acetoxypentyl)-3,17beta-bis-(tetrahydropyran-2-yloxy)-estra-1,3,5(10)-triene

시약·촉매·용매 2

HCID 8028
Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매

실험 절차

5.6 g of crude 7α-(5-acetoxypentyl)-estra-1,3,5(10)-triene-3,17β-diol is dissolved in 35 ml of anhydrous tetrahydrofuran and mixed with 3.5 ml of dihydropyran and 0.18 g of p-toluenesulfonic acid. The mixture is stirred at room temperature overnight, then diluted with ethyl acetate, and the mixture is shaken out in succession with saturated sodium bicarbonate solution and saturated common salt solution. The organic phase is dried with sodium sulfate and concentrated by evaporation in a vacuum, yield 8.31 g.

후처리

  1. dry with materialThe organic phase is dried with sodium sulfate
  2. concentrationconcentrated by evaporation in a vacuum, yield 8.31 g

출처 및 근거

ORD 기록
ord-2c7fd111ceec4178a1e198cbe9d41cfa
출처 데이터셋
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06288051B1

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