Hydrochloric Acid → n-Propyl 2-[4-(indan-2-yl-oxy)phenoxy]propionate

HRID 1388583

反応式

HRID 1388583 の反応式
CS([O:5][CH:6]1[CH2:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7]1)(=O)=O.C(=O)([O-])[O-].[K+].[K+].O[C:22]1[CH:36]=[CH:35][C:25]([O:26][CH:27]([CH3:34])[C:28]([O:30][CH2:31][CH2:32][CH3:33])=[O:29])=[CH:24][CH:23]=1.Cl>C(C(C)=O)C>[CH2:7]1[C:8]2[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:14][CH:6]1[O:5][C:22]1[CH:36]=[CH:35][C:25]([O:26][CH:27]([CH3:34])[C:28]([O:30][CH2:31][CH2:32][CH3:33])=[O:29])=[CH:24][CH:23]=1

参加物

6

実験手順

2-Methylsulphonyloxyindane (15.9 g) in methyl ethyl ketone (80 ml) was treated with potassium carbonate (15.53 g). The mixture was stirred and then n-propyl 2-(4-hydroxyphenoxy)propionate (16.8 g) in methyl ethyl ketone (20 ml) was added dropwise. The mixture was stirred at 90°-100° for 2.5 hours and was then poured into dilute hydrochloric acid. The mixture was extracted with ethyl acetate and the extract was washed thoroughly with water, dried and concentrated to an oil which semi-solidified on standing overnight. The oil was triturated with diethyl ether and petroleum ether. The mixture was filtered, and the filtrate concentrated to give an oil which was subjected to preparative thin layer chromatography on silica gel, eluting with chloroform/acetone/acetic acid (90:10:5), to give, as an oil, n-propyl 2-[4-(indan-2-yl-oxy)phenoxy]propionate (3.1 g).

後処理

  1. stirringThe mixture was stirred at 90°-100° for 2.5 hours
  2. extractionThe mixture was extracted with ethyl acetate
  3. washthe extract was washed thoroughly with water
  4. customdried
  5. concentrationconcentrated to an oil which
  6. customThe oil was triturated with diethyl ether and petroleum ether
  7. filtrationThe mixture was filtered
  8. concentrationthe filtrate concentrated
  9. customto give an oil which
  10. washeluting with chloroform/acetone/acetic acid (90:10:5)

出典と根拠

ORDレコード
ord-e17032d7efb74146a4cda5289f9988cf
出典データセット
uspto-grants-1984_02
特許番号
US04431834

関連ノート

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