Sodium borohydride → (5,6-Dimethoxy-3-(4-methyloxyphenoxy)-benzo[b]thiophen-2-yl)methanol

HRID 1004124

反応式

HRID 1004124 の反応式
[BH4-].[Na+].[CH3:3][O:4][C:5]1[C:24]([O:25][CH3:26])=[CH:23][C:8]2[S:9][C:10]([CH:21]=[O:22])=[C:11]([O:12][C:13]3[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=3)[C:7]=2[CH:6]=1>CO>[CH3:3][O:4][C:5]1[C:24]([O:25][CH3:26])=[CH:23][C:8]2[S:9][C:10]([CH2:21][OH:22])=[C:11]([O:12][C:13]3[CH:14]=[CH:15][C:16]([O:19][CH3:20])=[CH:17][CH:18]=3)[C:7]=2[CH:6]=1

参加物

4

反応物 2

HCID 4311764Sodium borohydride2 回HCID 110892155,6-Dimethoxy-3-(4-methoxyphenoxy)benzo[b]thiophene-2-carbaldehyde

生成物 1

HCID 18794388(5,6-Dimethoxy-3-(4-methyloxyphenoxy)-benzo[b]thiophen-2-yl)methanol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

26 mmol of NaBH4 are added at room temperature to a solution of 24 mmol of the compound obtained in Step E of Example 1 in 100 ml of methanol. After 2 hours' reaction, one equivalent of NaBH4 is added to the reaction mixture. After 12 hours' reaction, the solution is concentrated and then diluted with ethyl acetate, washed with a 1N HCl solution, then with water and then with a saturated NaCl solution, subsequently dried over calcium sulphate, filtered and concentrated under reduced pressure. Chromatography over silica gel (dichloromethane/ethyl acetate: 95/5) enables 6.07 g of the expected product to be isolated.

後処理

  1. additionis added to the reaction mixture
  2. customAfter 12 hours' reaction
  3. concentrationthe solution is concentrated
  4. additiondiluted with ethyl acetate
  5. washwashed with a 1N HCl solution
  6. dry with materialwith water and then with a saturated NaCl solution, subsequently dried over calcium sulphate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customto be isolated

出典と根拠

ORDレコード
ord-08dee4bf16114f4c80b7e9503bbda772
出典データセット
uspto-grants-2000_04
特許番号
US06048875

関連ノート

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