Water → HCID 22501140、化合物

HRID 1815670

反応式

HRID 1815670 の反応式
[CH3:1][C:2]([CH3:17])([CH2:15][OH:16])[CH:3]([C:5]1[CH:14]=[CH:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH:6]=1)[OH:4].C(N(CC)CC)C.[P:25](Cl)(Cl)([Cl:27])=[O:26].O>ClCCl>[Cl:27][P:25]1(=[O:26])[O:4][CH:3]([C:5]2[CH:14]=[CH:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[CH:6]=2)[C:2]([CH3:17])([CH3:1])[CH2:15][O:16]1

参加物

6

反応条件

温度
2.5 °C

実験手順

2,2-Dimethyl-1-(2-naphthyl)-1,3-propanediol (34.86 g, (0.151 mol) and triethylamine (42.9 g, 0.424 mol) were dissolved in dichloromethane (200 ml). Phosphorus oxychloride (24.3 g, 0.158 mol) dissolved in dichloromethane (50 ml) was added dropwise to the above solution under cooling to 1 to 4° C. with stirring for 1 hr 40 min. The solution was stirred at the same temperature for 1 hr, and water (60 ml) was added thereto to partition the solution. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. To the obtained dark brown oil was added ether (50 ml) and the mixture was stirred thoroughly and left at room temperature overnight. The solidified reaction product was pulverized, filtered, washed with ether and dried to give the title compound (38.62 g, yield 82.1%).

後処理

  1. additionwas added dropwise to the above solution
  2. stirringThe solution was stirred at the same temperature for 1 hr
  3. customto partition the solution
  4. washThe organic layer was washed with saturated brine
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. additionTo the obtained dark brown oil was added ether (50 ml)
  8. stirringthe mixture was stirred thoroughly
  9. waitleft at room temperature overnight
  10. filtrationfiltered
  11. washwashed with ether
  12. customdried

出典と根拠

ORDレコード
ord-ed68b3042d2b47d18e325f75acc2a22c
出典データセット
uspto-grants-2005_04
特許番号
US06878831B2

関連ノート

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