3-Methylnaphthalene-2-carboxylic acid → (3-Methylnaphthalen-2-yl)methanol

HRID 330521ノート

反応式

HRID 330521 の反応式
[CH3:1][C:2]1[C:3]([C:12](O)=[O:13])=[CH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[H-].[Al+3].[Li+].[H-].[H-].[H-]>C1COCC1>[CH3:1][C:2]1[C:3]([CH2:12][OH:13])=[CH:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2

参加物

4

反応条件

温度
0 °C

実験手順

A solution of 3-methyl-2-naphthoic acid (5.0 g, 26.9 mmol) in anhydrous THF (75 mL) was cooled to 0° C. and treated with lithium aluminum hydride (1M in THF, 26.9 mL, 26.9 mmol) added dropwise. After the addition was complete, the resulting mixture was stirred 5 minutes at 0° C., the ice bath was removed, the mixture warmed to room temperature and stirred a total of 20 hours. The mixture was cooled to 0° C. and quenched by dropwise addition of water (1.02 mL), followed by 15% NaOH (1.02 mL), and more water (3 mL). The resulting mixture was stirred 1 hour and the granular precipitate removed by filtration through a plug of Florosil and anhydrous magnesium sulfate. The filtrate was concentrated in vacuo, to give the desired product (4.6 g, 99%) as a white crystalline solid of sufficient purity for use in the subsequent reaction.

後処理

  1. additionadded dropwise
  2. additionAfter the addition
  3. customthe ice bath was removed
  4. temperaturethe mixture warmed to room temperature
  5. stirringstirred a total of 20 hours
  6. temperatureThe mixture was cooled to 0° C.
  7. customquenched by dropwise addition of water (1.02 mL)
  8. stirringThe resulting mixture was stirred 1 hour
  9. customthe granular precipitate removed by filtration through a plug of Florosil and anhydrous magnesium sulfate
  10. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-5d0a018efdcd4f4b87bd50640dfa4d04
出典データセット
uspto-grants-1990_01
特許番号
US04897405

反応ノート

読み込み中…