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3-Hydroxybenzaldehyde → 3-(Oxiran-2-ylmethoxy)benzaldehyde

HRID 1051436
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HRID 1051436 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[H-].[Na+].Cl[CH2:13][CH:14]1[CH2:16][O:15]1>CN(C=O)C>[O:15]1[CH2:16][CH:14]1[CH2:13][O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
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참가 물질

5

반응물 3

HCID 1013-HydroxybenzaldehydeHCID 7835EpichlorohydrinHCID 24758Sodium hydride

생성물 1

HCID 27740493-(Oxiran-2-ylmethoxy)benzaldehyde수율 75%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a solution of 3-hydroxybenzaldehyde (2.0 g, 16.38 mmol) in DMF (25 mL) was added NaH (60%, 982.6 mg, 24.57 mmol) at 0° C. in portions. The mixture was stirred at this temperature for 30 minutes before a solution of 2-(chloromethyl)oxirane (2.27 g, 24.57 mmol) in DMF (5 mL) was slowly added into the reaction mixture which was then allowed to reach room temperature slowly and stirred for 16 h. The solvent was removed by concentration and the residue dissolved in ethyl acetate and washed with water. T the separated organic layer was dried over sodium sulfate, filtered and concentrated. The crude product was then purified by column chromatography. (2.2 g, yield 75%) MS (ESI+) e/z: 179.1 [M+1]+.

후처리

  1. additionwas slowly added into the reaction mixture which
  2. customto reach room temperature
  3. customThe solvent was removed by concentration
  4. dissolutionthe residue dissolved in ethyl acetate
  5. washwashed with water
  6. dry with materialT the separated organic layer was dried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe crude product was then purified by column chromatography

출처 및 근거

ORD 기록
ord-ceddf5b7c0eb47bfba1a72bdf3c9dd5e
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09388173B2

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