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Acetic Acid → 5-Methoxynaphthalene-1-carbaldehyde

HRID 2060862
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HRID 2060862 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 962WaterHCID 14487Diisobutylaluminum hydrideHCID 13491715HCID 13491715, 화합물

생성물 1

HCID 115138875-Methoxynaphthalene-1-carbaldehyde

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
-78 °C

실험 절차

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]+.

후처리

  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)

출처 및 근거

ORD 기록
ord-c290f49081e24746842876c732e768dd
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08278442B2

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