Benzyl Chloride → HCID 15030177、化合物

HRID 248178

反応式

HRID 248178 の反応式
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([CH:12]([CH3:16])[C:13]([OH:15])=[O:14])[CH:6]=[CH:5]2.C[O-].[Na+].[CH2:20](Cl)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>CO>[CH3:16][CH:12]([C:7]1[CH:6]=[CH:5][C:4]2[C:9](=[CH:10][CH:11]=[C:2]([O:1][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:3]=2)[CH:8]=1)[C:13]([OH:15])=[O:14]

参加物

5

反応物 3

HCID 7503Benzyl ChlorideHCID 162920DesmethylnaproxenHCID 10942334Sodium Methoxide

生成物 1

HCID 15030177HCID 15030177、化合物収率 38.1%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 6-hydroxy-α-methyl-2-naphthaleneacetic acid (6.48 g, 30 mmol) in methanol (100 ml) is added sodium methoxide (60 mmol). After 10 minutes the solvent is removed and replaced with dimethylformamide (100 ml). Benzyl chloride (7.6 g, 60 mmol) is then added and the reaction mixture is stirred overnight at room temperature. The reaction is then heated at 150° C. for 1 hour. The solvent is then removed and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, dried over magnesium sulfate and evaporated to 11.5 g of crude product. This crude product is extracted with 100 ml hot hexane which affords 3.5 g of white crystals. A final recrystallization from methanol affords 2.5 g of white crystals of the intermediate ether ester (21% yield, m.p. 76°-78° C.).

後処理

  1. customAfter 10 minutes the solvent is removed
  2. temperatureThe reaction is then heated at 150° C. for 1 hour
  3. customThe solvent is then removed
  4. customthe residue is partitioned between water and methylene chloride
  5. washThe organic layer is washed with water
  6. dry with materialdried over magnesium sulfate
  7. customevaporated to 11.5 g of crude product
  8. extractionThis crude product is extracted with 100 ml hot hexane which

出典と根拠

ORDレコード
ord-a87f303f0be841629e4d49b56aa519a5
出典データセット
uspto-grants-1993_05
特許番号
US05208344

関連ノート

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