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Ethyl orthoformate → 3-(3-Diethoxymethyl-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

HRID 385126
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HRID 385126 반응식
C([C:3]1[CH:4]=[C:5]([CH:17]=[C:18]([C:22]([F:25])([F:24])[F:23])[C:19]=1[O:20][CH3:21])[C:6]([N:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[S:10][CH2:9]1)=[O:7])=O.[CH:26]([O:33][CH2:34][CH3:35])([O:30][CH2:31][CH3:32])OCC>C(O)C>[CH2:34]([O:33][CH:26]([O:30][CH2:31][CH3:32])[C:3]1[CH:4]=[C:5]([CH:17]=[C:18]([C:22]([F:23])([F:25])[F:24])[C:19]=1[O:20][CH3:21])[C:6]([N:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[S:10][CH2:9]1)=[O:7])[CH3:35]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 31214Ethyl orthoformateHCID 866681793-(3-Formyl-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

생성물 1

HCID 681089993-(3-Diethoxymethyl-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3-(3-formyl-4-methoxy-5-trifluoromethylbenzoyl)-2,3-dihydro-1,3-benzothiazole (277 mg) was dissolved in ethanol (1.5 mL) and triethyl orthoformate (0.16 mL), Amberlyst-15 (27 mg) was added to the solution, and then the mixture was refluxed for 3.5 hours. The reaction solution was filtered, and then the solvent was distilled off under reduced pressure to obtain the title compound (326 mg) as a yellow oily substance.

후처리

  1. temperaturethe mixture was refluxed for 3.5 hours
  2. filtrationThe reaction solution was filtered
  3. distillationthe solvent was distilled off under reduced pressure

출처 및 근거

ORD 기록
ord-09e14a49c86c425fa3759f2bdd811d9b
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08367843B2

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