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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-[3-(2-Carboxycyclohexylmethyloxy)phenyl]propionic acid → 2-(6,6a,7,8,9,10,10a,11-Octahydro-11-oxodibenz[b,e]oxepin-3-yl)propionic acid

HRID 223714
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HRID 223714 반응식
[C:1]([CH:4]1[CH2:9][CH2:8][CH2:7][CH2:6][CH:5]1[CH2:10][O:11][C:12]1[CH:13]=[C:14]([CH:18]([CH3:22])[C:19]([OH:21])=[O:20])[CH:15]=[CH:16][CH:17]=1)([OH:3])=O>O>[O:3]=[C:1]1[CH:4]2[CH2:9][CH2:8][CH2:7][CH2:6][CH:5]2[CH2:10][O:11][C:12]2[CH:13]=[C:14]([CH:18]([CH3:22])[C:19]([OH:21])=[O:20])[CH:15]=[CH:16][C:17]1=2
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참가 물질

3

반응물 1

HCID 128324962-[3-(2-Carboxycyclohexylmethyloxy)phenyl]propionic acid

생성물 1

HCID 128325042-(6,6a,7,8,9,10,10a,11-Octahydro-11-oxodibenz[b,e]oxepin-3-yl)propionic acid수율 8%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
100 °C

실험 절차

2-[3-(2-Carboxycyclohexylmethyloxy)phenyl]propionic acid (14 g) was added to polyphophoric acid (80 g) and the mixture was heated with stirring for 2.5 hours in an oil bath maintained at 100° C. The reaction mixture was diluted with water and extracted with ethyl acetate. The ethyl acetate layers were washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure. The residue was chromatographed on silica gel, using methanol-chloroform (2:98, v/v) as an eluent, to give 2-(6,6a,7,8,9,10,10a,11-octahydro-11-oxodibenz[b,e]oxepin-3-yl)propionic acid (1.05 g) as an oil. IR νmaxfilm cm-1 : 1700, 1680 (C=O). HRMS m/e: 288.1390 (M+) (Molecular weight calculated for C17H20O4 : 288.1362).

후처리

  1. temperaturethe mixture was heated
  2. extractionextracted with ethyl acetate
  3. washThe ethyl acetate layers were washed with water
  4. dry with materialdried over anhydrous sodium sulfate
  5. customevaporated to dryness under reduced pressure
  6. customThe residue was chromatographed on silica gel

출처 및 근거

ORD 기록
ord-a1e43198f3d9409c922b6bfdc2cb541a
출처 데이터셋
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04356186

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