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Sodium Acetate → 2-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene

HRID 844155
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HRID 844155 반응식
[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]([CH2:11]Cl)[C:9]=1[Cl:10])=[O:4].[C:13]([O-:16])(=[O:15])[CH3:14].[Na+]>C(O)(=O)C>[CH3:1][O:2][C:3]([C:5]1[S:6][CH:7]=[C:8]([CH2:11][O:16][C:13](=[O:15])[CH3:14])[C:9]=1[Cl:10])=[O:4]
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참가 물질

4

반응물 2

HCID 517045Sodium AcetateHCID 183767792-Methoxycarbonyl-3-chloro4-(chloromethyl)thiophene

생성물 1

HCID 183769232-Methoxycarbonyl-3-chloro4-(acetoxymethyl)thiophene수율 90%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To 2-methoxycarbonyl-3-chloro-4-(chloromethyl)thiophene (48 g, 0.21 mol) in glacial acetic acid (500 mL) was added sodium acetate (35 g, 0.42 mol). The reaction was heated at reflux for 24 hours, then cooled and concentrated in vacuo. The residual oil was made basic by addition of saturated aqueous sodium bicarbonate, and the resulting solution extracted with ethyl acetate (4×150 mL). The combined extracts were dried over sodium sulfate and concentrated to afford 47 g (90% yield) of 2-methoxycarbonyl-3-chloro-4-(acetoxymethyl)thiophene as a light brown oil; NMR (CDCl3) 7.6 (s, 1), 5.1 (s, 2), 3.9 (s, 3), 2.1 (s, 3) ppm.

후처리

  1. temperatureThe reaction was heated
  2. temperatureat reflux for 24 hours
  3. temperaturecooled
  4. concentrationconcentrated in vacuo
  5. additionThe residual oil was made basic by addition of saturated aqueous sodium bicarbonate
  6. extractionthe resulting solution extracted with ethyl acetate (4×150 mL)
  7. dry with materialThe combined extracts were dried over sodium sulfate
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-14e39ad2b34c465a93664b1f7bfab173
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06380221B1

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