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Tetrahydrofuran → (2-Methoxy-4-propylphenyl)methanol

HRID 2035415
ノート
印刷プレビュー

反応式

HRID 2035415 の反応式
COCCO[AlH2-]O[CH2:8][CH2:9][O:10][CH3:11].[Na+].[C:13]1(C)[CH:18]=CC=[CH:15][CH:14]=1.[O:20]1[CH2:24][CH2:23][CH2:22][CH2:21]1.O.O.O.O.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>CO>[CH3:11][O:10][C:9]1[CH:8]=[C:18]([CH2:13][CH2:14][CH3:15])[CH:24]=[CH:23][C:22]=1[CH2:21][OH:20]
参加物反応条件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 8028TetrahydrofuranHCID 2724148Sodium potassium tartrate tetrahydrateHCID 131728749Red-Al toluene

生成物 1

HCID 59582157(2-Methoxy-4-propylphenyl)methanol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
35 °C

実験手順

Red-Al/toluene solution (66.5% content, 2.05 g) was slowly added to a tetrahydrofuran (3 mL) solution of the compound (1.00 g) prepared in Example 43 at an internal temperature of 5° C., followed by stirring at an internal temperature of about 35° C. for about 2.5 hours. Methanol (0.5 mL) was added to the reaction solution at an internal temperature of 9° C. to stop the reaction. The reaction solution was poured into a 50% aqueous potassium sodium tartrate tetrahydrate solution, and extracted with ethyl acetate. The organic layer was successively washed with water and brine, dried, and concentrated, to thereby obtain the title compound (0.91 g) having the following physical properties.

後処理

  1. customthe reaction
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was successively washed with water and brine
  4. customdried
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-cc42a6dc83f74acfa2de7125f2bd3e89
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08575134B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート