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Water → 6-Methyl-2-methylaminobenzyl alcohol

HRID 1762184
ノート
印刷プレビュー

反応式

HRID 1762184 の反応式
[CH:1]([NH:3][C:4]1[CH:11]=[CH:10][CH:9]=[C:8]([CH3:12])[C:5]=1[CH2:6][OH:7])=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].O>O1CCCC1>[CH3:12][C:8]1[C:5]([CH2:6][OH:7])=[C:4]([NH:3][CH3:1])[CH:11]=[CH:10][CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 143684522-Formamido-6-methylbenzyl alcoholHCID 21226445Aluminium lithium hydride

生成物 1

HCID 540947806-Methyl-2-methylaminobenzyl alcohol収率 49.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of 2-formamido-6-methylbenzyl alcohol (1.9 g) in tetrahydrofuran (26 ml) was added dropwise to a suspension of lithium aluminum hydride (0.873 g) in tetrahydrofuran (17 ml) at room temperature over a period of 10 minutes. After being refluxed for 4.5 hours, the excess reagent was decomposed with a small amount of water and the resulting precipitates were filtered off by suction. The filtrate was evaporated in vacuo and the residue was recrystallized from carbon tetrachloride to give 6-methyl-2-methylaminobenzyl alcohol (0.86 g).

後処理

  1. temperatureAfter being refluxed for 4.5 hours
  2. customthe resulting precipitates
  3. filtrationwere filtered off by suction
  4. customThe filtrate was evaporated in vacuo
  5. customthe residue was recrystallized from carbon tetrachloride

出典と根拠

ORDレコード
ord-d1b51f6357394f49aaea3d7e4e62f200
出典データセット
uspto-grants-1989_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04831041

反応ノート

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