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p-Toluenesulfonic acid → HCID 18595306、化合物

HRID 1580574
ノート
印刷プレビュー

反応式

HRID 1580574 の反応式
[Cl:1][C@H:2]1[CH2:22][C@@:21]2([CH3:23])[C@@H:13]([CH2:14][C@H:15]([CH3:25])[C@:16]2([OH:24])[C:17](=[O:20])[CH2:18][OH:19])[C@H:12]2[C@H:3]1[C@:4]1([CH3:27])[C:9]([CH2:10][CH2:11]2)=[CH:8][C:7](=[O:26])[CH:6]=[CH:5]1.[C:28](OC)(OC)([O:32]C)[CH:29]([CH3:31])[CH3:30].C1(C)C=CC(S(O)(=O)=O)=CC=1.C(=O)(O)[O-].[Na+]>O1CCOCC1.CC(C)=O.O>[Cl:1][C@H:2]1[CH2:22][C@@:21]2([CH3:23])[C@@H:13]([CH2:14][C@H:15]([CH3:25])[C@:16]2([O:24][C:28](=[O:32])[CH:29]([CH3:31])[CH3:30])[C:17](=[O:20])[CH2:18][OH:19])[C@H:12]2[C@H:3]1[C@:4]1([CH3:27])[C:9]([CH2:10][CH2:11]2)=[CH:8][C:7](=[O:26])[CH:6]=[CH:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 6101p-Toluenesulfonic acidHCID 404951,1,1-Trimethoxy-2-methylpropaneHCID 516892Sodium Bicarbonate2 回HCID 18595305(11β,16β)-11-Chloro-17,21-dihydroxy-16-methylpregna-1,4-diene-3,20-dione

生成物 1

HCID 18595306HCID 18595306、化合物

試薬・触媒・溶媒 3

HCID 180
Acetone
溶媒
HCID 962Water溶媒
HCID 312751,4-Dioxane溶媒

実験手順

A solution of 11β-chloro-17,21-dihydroxy-16β-methylpregna-1,4-diene-3,20-dione (214 mg.) in dioxan (7 ml.) was treated with trimethyl orthoisobutyrate (0.22 ml.) and toluene p-sulphonic acid (23 mg.) at room temperature. After 45 minutes a little sodium bicarbonate was added and the mixture was then poured into a dilute solution of sodium bicarbonate. The oily product was extracted into ethyl acetate and washed with water. Evaporation of the organic solent gave an oil which was dissolved in acetone (10 ml.) and treated with 0.08 N-sulphuric acid (2.4 ml.). After keeping at room temperature for 30 minutes, the solution was diluted with water and the precipitated oil was extracted with ethyl acetate and washed with water. Evaporation of the organic solvent afforded the crude product which, on crystallization from ether-petroleum ether, gave the title compound, m.p. 163°-164° (K), [α]D + 108.5 (c 0.6 chloroform) λmax 240 nm (ε 15,460) (Found: C, 67.7; H, 7.7; Cl, 7.4. C26H35Cl O5 requires C, 67.45; H, 7.6; Cl, 7.65%).

後処理

  1. extractionThe oily product was extracted into ethyl acetate
  2. washwashed with water
  3. customEvaporation of the organic solent
  4. customgave an oil which
  5. extractionthe precipitated oil was extracted with ethyl acetate
  6. washwashed with water
  7. customEvaporation of the organic solvent
  8. customafforded the crude product which
  9. customon crystallization from ether-petroleum ether

出典と根拠

ORDレコード
ord-8234be8e7c69430f95f2821e3c553ecb
出典データセット
uspto-grants-1976_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03933799

反応ノート

読み込み中…

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