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Acetic Acid → 5-Methoxynaphthalene-1-carbaldehyde

HRID 2060862
ノート
印刷プレビュー

反応式

HRID 2060862 の反応式
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[C:8]2[C:13]#N.CC(C[AlH]CC(C)C)C.C(O)(=[O:26])C.O>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:4]=1[CH:5]=[CH:6][CH:7]=[C:8]2[CH:13]=[O:26]
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

6

反応物 4

HCID 176Acetic AcidHCID 962WaterHCID 14487Diisobutylaluminum hydrideHCID 13491715HCID 13491715、化合物

生成物 1

HCID 115138875-Methoxynaphthalene-1-carbaldehyde

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
-78 °C

実験手順

To a solution of 5-methoxynaphthalene-1-carbonitrile (Preparation 11) (1.1 g, 6.00 mmol) in DCM (40 mL) at −78° C. under nitrogen was added DIBAL (1.0M in toluene, 18 mL) dropwise over 10 minutes. The reaction mixture was stirred at −78° C. for 1 h, warmed to rt for 1 h and then cooled to 0° C. Acetic acid (1 mL) followed by water (1 mL) were added. The mixture was partitioned between EtOAc (100 mL) and water (100 mL), the organic phase was separated and dried (MgSO4). Solvent was removed in vacuo and the residue purified by column chromatography (EtOAc:isohexane 2:8) to give the title compound: RT=3.54 min; m/z (ES+)=187.0 [M+H]+.

後処理

  1. temperaturewarmed to rt for 1 h
  2. temperaturecooled to 0° C
  3. additionwere added
  4. customThe mixture was partitioned between EtOAc (100 mL) and water (100 mL)
  5. customthe organic phase was separated
  6. dry with materialdried (MgSO4)
  7. customSolvent was removed in vacuo
  8. customthe residue purified by column chromatography (EtOAc:isohexane 2:8)

出典と根拠

ORDレコード
ord-c290f49081e24746842876c732e768dd
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08278442B2

反応ノート

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