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Water → (3-Chloro-2-methylphenyl)methanol

HRID 1042349
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HRID 1042349 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].C[O:8][C:9](=O)[C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([Cl:16])[C:11]=1[CH3:17].O>C1COCC1>[Cl:16][C:12]1[C:11]([CH3:17])=[C:10]([CH2:9][OH:8])[CH:15]=[CH:14][CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 5077673Methyl 3-chloro-2-methylbenzoateHCID 21226445Aluminium lithium hydride

생성물 1

HCID 13169022(3-Chloro-2-methylphenyl)methanol수율 103.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

LAH (61.00 mL, 1.0 M in THF, 61.00 mmol) was added to a solution of 3-chloro-2-methyl-benzoic acid methyl ester (4.50 g, 24.40 mmol) in THF at 0° C. The reaction mixture was stirred for 1 hour, water was added to quench the reaction. The aqueous layer was extracted with Et2O (3×150 mL), and the combined organic phases were washed with brine (1×150 mL) and dried over MgSO4. Purification by column chromatography using hex:EtOAc (4:1) as the eluant afforded 3.97 g of the title compound. Spectroscopic data: 1H NMR (300 MHz, CDCl3.) δ 1.94 (br s, 1H), 2.36 (s, 3H), 4.67 (br s, 2H), 7.11 (t, J=7.765 Hz, 1H), 7.245 (d, J=7.03 Hz, 1H), 7.30 (d, J=7.91 Hz, 1H).

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후처리

  1. customto quench
  2. customthe reaction
  3. extractionThe aqueous layer was extracted with Et2O (3×150 mL)
  4. washthe combined organic phases were washed with brine (1×150 mL)
  5. dry with materialdried over MgSO4
  6. customPurification by column chromatography

출처 및 근거

ORD 기록
ord-d4d8729ed4114d8ebe420d370e76668a
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557853B2

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