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Acetyl chloride → 2-Formyl-5-methylphenyl acetate

HRID 1773211
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HRID 1773211 반응식
[OH:1][C:2]1[CH:9]=[C:8]([CH3:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[C:11](Cl)(=[O:13])[CH3:12]>C(Cl)Cl>[C:11]([O:1][C:2]1[CH:9]=[C:8]([CH3:10])[CH:7]=[CH:6][C:3]=1[CH:4]=[O:5])(=[O:13])[CH3:12]
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참가 물질

4

반응물 2

HCID 6367Acetyl chlorideHCID 612002-Hydroxy-4-methylbenzaldehyde

생성물 1

HCID 538517102-Formyl-5-methylphenyl acetate수율 91.8%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
2.5 °C

실험 절차

To a 0-5° C. solution of 2-hydroxy-4-methylbenzaldehyde (15 g, 110 mmol) in 250 mL of DCM was added TEA (30.7 ml, 220 mmol) followed by dropwise addition of acetyl chloride (8.65 g, 110 mmol) over 15 min. The reaction was stirred at 0-5° C. for 30 min. The reaction mixture was concentrated under reduced pressure. To this residue 100 mL of 1N HCl was added. The crude mixture was extracted with EtOAc×2. The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to give a yellow oil, 2-formyl-5-methylphenyl acetate (18 g). 1H NMR (400 MHz, DMSO-d6) δ 2.34 (s, 3H), 2.40 (s, 3H), 7.13 (s, 1H), 7.31 (d, J=7.6 Hz, 1H), 7.80 (d, J=7.8 Hz, 1H), 10.01 (s, 1H).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. additionTo this residue 100 mL of 1N HCl was added
  3. extractionThe crude mixture was extracted with EtOAc×2
  4. washThe combined organic layers were washed with brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-2361d1ba117a4316a9b84bf4c6474b60
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09255093B2

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