Dimethylformamide → HCID 22457522, 화합물

HRID 1597135노트

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HRID 1597135 반응식
[C:1]([O:4][CH2:5][CH2:6][C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([S:17]([O-:20])(=O)=[O:18])=[CH:9][CH:8]=1)(=[O:3])[CH3:2].[K+].CN(C)C=O.S(Cl)([Cl:29])=O>>[C:1]([O:4][CH2:5][CH2:6][C:7]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]([S:17]([Cl:29])(=[O:20])=[O:18])=[CH:9][CH:8]=1)(=[O:3])[CH3:2]

참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 23713435HCID 23713435, 화합물

생성물 1

HCID 22457522HCID 22457522, 화합물수율 80.4%

반응 조건

온도
80 °C

실험 절차

Potassium 4-(2-acetoxy-ethyl)-naphthalene-1-sulfonate (102.3 g, 308 mmol) was added in portions over 15 minutes to a room temperature solution of dimethylformamide (2.4 mL, 31 mmol) in thionyl chloride (112 mL, 1.54 mol). The reaction mixture was gradually brought to 80 ° C. (oil bath temperature) over 30 minutes and heated at 80° C. for 90 minutes, then cooled to room temperature and stirred at room temperature for 60 minutes. The reaction mixture was partitioned between ice water (500 mL) and ethyl acetate (500 mL). The organic layer was washed with water (200 mL) and brine (200 mL), dried over magnesium sulfate, filtered, and evaporated under vacuum to a cream colored solid. The crude product was triturated with pet ether to afford 4-(2-acetoxy-ethyl)-naphthalene-1-sulfonyl chloride as a pale tan solid (77.47 g).

후처리

  1. customwas gradually brought to 80 ° C.
  2. customover 30 minutes
  3. temperaturecooled to room temperature
  4. customThe reaction mixture was partitioned between ice water (500 mL) and ethyl acetate (500 mL)
  5. washThe organic layer was washed with water (200 mL) and brine (200 mL)
  6. dry with materialdried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated under vacuum to a cream
  9. customThe crude product was triturated with pet ether

출처 및 근거

ORD 기록
ord-9860f97cf89f43b988295c6120c0b93d
출처 데이터셋
uspto-grants-2001_09
특허 번호
US06294529B1

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