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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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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
ノート
印刷プレビュー

反応式

HRID 223714 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-a1e43198f3d9409c922b6bfdc2cb541a
出典データセット
uspto-grants-1982_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04356186

反応ノート

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