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Diisobutylaluminum hydride → (3,4-Dimethoxy-5-propylphenyl)methanol

HRID 638911
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HRID 638911 반응식
C[O:2][C:3](=O)[C:4]1[CH:9]=[C:8]([CH2:10][CH2:11][CH3:12])[C:7]([O:13][CH3:14])=[C:6]([O:15][CH3:16])[C:5]=1C.CC(C[AlH]CC(C)C)C.C(C(C(C([O-])=O)O)O)([O-])=O.[K+].[K+]>C(Cl)Cl>[CH3:16][O:15][C:6]1[CH:5]=[C:4]([CH:9]=[C:8]([CH2:10][CH2:11][CH3:12])[C:7]=1[O:13][CH3:14])[CH2:3][OH:2]
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5

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HCID 14487Diisobutylaluminum hydrideHCID 6100505Dipotassium 2,3-dihydroxybutanedioateHCID 86618865Methyl 3,4-dimethoxy-5-propylbenzoic acid methyl ester

생성물 1

HCID 19838159(3,4-Dimethoxy-5-propylphenyl)methanol수율 102.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
-78 °C

실험 절차

To a stirred solution of methyl 3,4-dimethoxy-5-propylbenzoic acid methyl ester (Example 1, Step 4, 6.0 g, 25.2 mmol) in DCM (400 mL) at −78° C. was added DIBAH (1.0 M in toluene, 76 mL, 76 mmol). The reaction mixture was stirred at −78° C. for 30 min then quenched with EtOAc (50 mL). The quenched reaction was warmed to room temperature then treated with 1:1 saturated aqueous potassium tartrate/saturated aqueous sodium bicarbonate (400 mL). The biphasic mixture was stirred vigorously for 30 min then the layers separated. The aqueous layer was extracted with EtOAc (300 mL), then the combined organic layer was dried over MgSO4, and concentrated to give 3,4-dimethoxy-5-propylbenzylalcohol (5.42 g, 100% yield). The product was used without further purification.

후처리

  1. customthen quenched with EtOAc (50 mL)
  2. customThe quenched reaction
  3. temperaturewas warmed to room temperature
  4. stirringThe biphasic mixture was stirred vigorously for 30 min
  5. customthe layers separated
  6. extractionThe aqueous layer was extracted with EtOAc (300 mL)
  7. dry with materialthe combined organic layer was dried over MgSO4
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f112ff438b484893967950e6ccf665cb
출처 데이터셋
uspto-grants-2010_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07691843B2

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