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Oxalic acid dihydrate → Estra-5(10),16-dien-3-one

HRID 1108453
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HRID 1108453 반응식
C[O:2][C:3]1[CH2:21][CH2:20][C@@:19]2(C)[C:5](=[CH:6][CH2:7][C@@H:8]3[C@@H:18]2[CH2:17][CH2:16][C@@:15]2([CH3:23])[C@H:9]3[CH2:10][CH2:11][C@@H:12]2C=C)[CH:4]=1.O.O.C(O)(=O)C(O)=O>CC(C)=O>[CH3:23][C@:15]12[CH2:16][CH2:17][C@H:18]3[C@@H:8]([CH2:7][CH2:6][C:5]4[CH2:4][C:3](=[O:2])[CH2:21][CH2:20][C:19]=43)[C@@H:9]1[CH2:10][CH:11]=[CH:12]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 61373Oxalic acid dihydrateHCID 57012029Pregna-3,5,20-trien-3-yl methyl ether

생성물 1

HCID 15870993Estra-5(10),16-dien-3-one수율 75.5%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

Estra-2,5(10), 16-triene-3-methyl ether (2) (646.3 mg, 2.390 mmole), dissolved in 50 ml of acetone was hydrolyzed for 6 h at room temperature using oxalic acid dihydrate (0.84 g, 6.7 mmole). The reaction mixture was quenched with 25 ml of saturated sodium bicarbonate and then extracted twice with 25 ml portions of ethyl acetate. The combined organic extracts were washed twice with 25 ml of brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was recrystallized from hexane to give product (462.5 mg, 1.804 mmole, 75%), m.p. 112-116 C.

후처리

  1. customThe reaction mixture was quenched with 25 ml of saturated sodium bicarbonate
  2. extractionextracted twice with 25 ml portions of ethyl acetate
  3. washThe combined organic extracts were washed twice with 25 ml of brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was recrystallized from hexane

출처 및 근거

ORD 기록
ord-059d685fddf542ae90ac161892f487f6
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06066627

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