2-Benzyloxyphenol → HCID 66894914、化合物

HRID 19245

反応式

HRID 19245 の反応式
CC(C)([O-])C.[K+].[CH2:7]([O:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[OH:21])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH2:22]([O:24][C:25](=[O:30])[CH:26]=[C:27](Cl)[CH3:28])[CH3:23]>O1CCCC1>[CH2:22]([O:24][C:25](=[O:30])/[CH:26]=[C:27](/[O:21][C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[O:14][CH2:7][C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1)\[CH3:28])[CH3:23]

参加物

5

反応条件

温度
23 °C

実験手順

Potassium t-butoxide (5.60 g, 0.05 mol) was added to a stirred solution of 2-benzyloxy-phenol (5.00 g, 0.025 mol) in tetrahydrofuran (50 mL) at 23° C. under nitrogen and the reaction mixture was heated to reflux for 0.75 h. The reaction mixture was cooled to 23° C. and a solution of 3-chloro-but-2-enoic acid ethyl ester (prepared as in Example 191, 3.70 g, 0.025 mol) in tetrahydrofuran (40 mL) was added to the reaction mixture. The reaction mixture was refluxed for an additional 3 h. After this time, the mixture was concentrated in vacuo and the residue was diluted with water and extracted with diethyl ether. The organic layer was then washed with 5% aqueous sodium hydroxide solution followed by a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated in vacuo to afford (E)-3-(2-benzyloxy-phenoxy)-but-2-enoic acid ethyl ester (5.70 g, 73%) as a yellow oil.

後処理

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux for 0.75 h
  3. temperatureThe reaction mixture was refluxed for an additional 3 h
  4. concentrationAfter this time, the mixture was concentrated in vacuo
  5. additionthe residue was diluted with water
  6. extractionextracted with diethyl ether
  7. washThe organic layer was then washed with 5% aqueous sodium hydroxide solution
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-cdc7cce75ed845c496478ac8e38edcf1
出典データセット
uspto-grants-2010_06
特許番号
US07741327B2

関連ノート

読み込み中…