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Phosphoric Acid → Methyl 2-(5-acetylthiophen-2-yl)acetate

HRID 262025
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HRID 262025 반응식
[CH3:1][O:2][C:3](=[O:10])[CH2:4][C:5]1[S:6][CH:7]=[CH:8][CH:9]=1.[C:11](OC(=O)C)(=[O:13])[CH3:12].OP(O)(O)=O>>[CH3:1][O:2][C:3](=[O:10])[CH2:4][C:5]1[S:6][C:7]([C:11](=[O:13])[CH3:12])=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1004Phosphoric AcidHCID 7918Acetic AnhydrideHCID 88055Methyl thiophen-2-acetate

생성물 1

HCID 54189483Methyl 2-(5-acetylthiophen-2-yl)acetate

실험 절차

A mixture of 2-thienylacetic acid methyl ester, 1.41 g. (0.01 mol) and acetic anhydride, 4.2 g. (0.04 mol) was heated at 70°-80° C. and 0.2 g. of 85% H3PO4 was added dropwise with mechanically stirring. The reaction was somewhat exothermic but cooling was not necessary. The mixture was maintained between 70°-80° C. for 3 hours, and then, poured onto ice-water followed by extraction with ether. Organic layer was washed with water several times, dried over anhyd. MgSO4 and evaporated. The residue was distilled at 2mmHg and a fraction between 160° C. and 172° C. was collected. This material was gradually crystallized and could be recrystallized from the mixture of light-petroleum and benzene. m.p. 43°-44° C. Yield; 1.39 g. (76.5%)

후처리

  1. temperature(0.04 mol) was heated at 70°-80° C.
  2. temperaturecooling
  3. temperatureThe mixture was maintained between 70°-80° C. for 3 hours
  4. additionpoured onto ice-water
  5. extractionfollowed by extraction with ether
  6. washOrganic layer was washed with water several times
  7. customdried over anhyd
  8. customMgSO4 and evaporated
  9. distillationThe residue was distilled at 2mmHg
  10. customa fraction between 160° C. and 172° C. was collected
  11. customThis material was gradually crystallized
  12. customcould be recrystallized from the mixture of light-petroleum and benzene

출처 및 근거

ORD 기록
ord-d31927f280704f32b6ff0ec89291d5b7
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04153610

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