Pyridine → 4-[3-Tert.butyl-4-methoxybenzoylthio]benzoic acid

HRID 1681572ノート

反応式

HRID 1681572 の反応式
[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]=1[O:14][CH3:15])[C:8]([OH:10])=O)([CH3:4])([CH3:3])[CH3:2].[SH:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([OH:23])=[O:22])=[CH:19][CH:18]=1.N1C=CC=CC=1>ClCCl>[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[CH:12][C:13]=1[O:14][CH3:15])[C:8]([S:16][C:17]1[CH:25]=[CH:24][C:20]([C:21]([OH:23])=[O:22])=[CH:19][CH:18]=1)=[O:10])([CH3:2])([CH3:3])[CH3:4]

参加物

5

反応物 3

HCID 1049PyridineHCID 957384-Mercaptobenzoic acidHCID 10488578Benzoic acid, 3-(1,1-dimethylethyl)-4-methoxy-2 回

生成物 1

HCID 198051694-[3-Tert.butyl-4-methoxybenzoylthio]benzoic acid収率 32%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Crude 3-(tert.butyl)-4-methoxybenzoic acid, prepared starting with 1.04 g (5 mmoles) of 3-(tert.butyl)-4-methoxybenzoic acid, described in Example 35 of French Patent No. 85 13747 (2.570.377), is dissolved in 15 ml of dichloromethane. The solution is slowly added to a mixture of 771 mg (5 mmoles) of 4-mercaptobenzoic acid and 8 ml of pyridine. The reaction mixture is stirred at ambient temperature for 8 hours, evaporated to dryness, taken up in water, acidified to pH 5 with 1N HCl and extracted with ethyl ether. The organic phase is decanted, washed with water, dried over magnesium sulfate and evaporated to dryness. The resulting residue is purified by chromatography on a silica column (eluant: ethyl ether). The solvent is evaporated and 530 mg (32% yield) of 4-[3-tert.butyl-4-methoxybenzoylthio]benzoic acid whose melting point is 220°-221° C. are obtained.

後処理

  1. customevaporated to dryness
  2. extractionextracted with ethyl ether
  3. customThe organic phase is decanted
  4. washwashed with water
  5. dry with materialdried over magnesium sulfate
  6. customevaporated to dryness
  7. customThe resulting residue is purified by chromatography on a silica column (eluant: ethyl ether)
  8. customThe solvent is evaporated

出典と根拠

ORDレコード
ord-4ca641af673646629be97e70c6a50fcf
出典データセット
uspto-grants-1992_12
特許番号
US05173289

反応ノート

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