Nitrogen → Methyl (3β)-3-hydroxy-7-oxochol-5-en-24-oate

HRID 1456006ノート

反応式

HRID 1456006 の反応式
C([O-])([O-])=O.[K+].[K+].C([O:10][C@H:11]1[CH2:35][CH2:34][C@@:33]2([CH3:36])[C:13](=[CH:14][C:15](=[O:38])[C@@H:16]3[C@@H:32]2[CH2:31][CH2:30][C@@:29]2([CH3:37])[C@H:17]3[CH2:18][CH2:19][C@@H:20]2[C@H:21]([CH3:28])[CH2:22][CH2:23][C:24]([O:26][CH3:27])=[O:25])[CH2:12]1)(=O)C.N#N>CO>[OH:10][C@H:11]1[CH2:35][CH2:34][C@@:33]2([CH3:36])[C:13](=[CH:14][C:15](=[O:38])[C@@H:16]3[C@@H:32]2[CH2:31][CH2:30][C@@:29]2([CH3:37])[C@H:17]3[CH2:18][CH2:19][C@@H:20]2[C@H:21]([CH3:28])[CH2:22][CH2:23][C:24]([O:26][CH3:27])=[O:25])[CH2:12]1

参加物

5

反応物 3

HCID 947NitrogenHCID 11430Potassium CarbonateHCID 23250093HCID 23250093、化合物

生成物 1

HCID 23250094Methyl (3β)-3-hydroxy-7-oxochol-5-en-24-oate

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a suspension of finely ground K2CO3 (3.45 g , 25 mmoles) in 250 ml of methanol was added methyl 3β-acetoxy-7-oxochol-5-en-24-oate (1) (11.1 g, 25 mmoles). After stirring at 450° for 15 min in a N2 atmosphere, most of the methanol was removed in vacuo from the clear brown reaction mixture. The residue was suspended in H2O and extracted three times with CH2Cl2. The combined extracts were washed with H2O twice and saturated brine and dried with MgSO4. Evaporation in vacuo gave 10.1 g of nearly pure 2 as a pale yellow solid. The nuclear magnetic resonance data for this and subsequent Examples was taken at 400 MHz in CDCl3 : δ 0.68 (s, 3H, 18-Me); 0.94 (d, 3H, 20-Me); 1.21 (s, 3H, 19-Me); 3.66 (s, 3H, CO2Me); 3.68 (m, 1H, 3-H); 5.70 (s, 1H, 6-H).

後処理

  1. customwas removed in vacuo from the clear brown reaction mixture
  2. extractionextracted three times with CH2Cl2
  3. washThe combined extracts were washed with H2O twice
  4. dry with materialsaturated brine and dried with MgSO4
  5. customEvaporation in vacuo

出典と根拠

ORDレコード
ord-53946114295e4e8e87bcdc95170d2345
出典データセット
uspto-grants-1998_12
特許番号
US05843953

反応ノート

読み込み中…