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Methanol → HCID 54182122, 화합물

HRID 972360
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HRID 972360 반응식
[F:1][C:2]1[CH:7]=[C:6]([CH2:8][C:9]([OH:11])=[O:10])[CH:5]=[CH:4][C:3]=1[C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][C:13]=1[F:19].[CH3:20]O>S(=O)(=O)(O)O>[F:1][C:2]1[CH:7]=[C:6]([CH2:8][C:9]([O:11][CH3:20])=[O:10])[CH:5]=[CH:4][C:3]=1[C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][C:13]=1[F:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 887MethanolHCID 21406751HCID 21406751, 화합물

생성물 1

HCID 54182122HCID 54182122, 화합물

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

A solution of 2,2',4'-trifluoro-4-biphenylyl acetic acid (10 g.) in anhydrous methanol (100 ml.) and concentrated sulphuric acid (5 ml.) was refluxed overnight. Excess solvent was distilled and the residue was poured onto ice-water and extracted with ether. The extracts were washed with dilute aqueous sodium bicarbonate and then dried, evaporated and distilled to give a yellow oil, b.p. 142°-146°/0.5 mm., which solidified on cooling. This was crystallized from 62-68 petroleum ether to give methyl 2,2',4'-trifluoro-4-biphenylylacetate, m.p. 74°-77° C.

후처리

  1. distillationExcess solvent was distilled
  2. additionthe residue was poured onto ice-water
  3. extractionextracted with ether
  4. washThe extracts were washed with dilute aqueous sodium bicarbonate
  5. customdried
  6. customevaporated
  7. distillationdistilled
  8. customto give a yellow oil, b.p. 142°-146°/0.5 mm
  9. temperatureon cooling
  10. customThis was crystallized from 62-68 petroleum ether

출처 및 근거

ORD 기록
ord-22ea3e4e51eb4f7ba8f773ba3f78b091
출처 데이터셋
uspto-grants-1977_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04052514

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