Water → 2-Hydroxy-9-carboxy-10,11-dihydrodibenzo[b,f]thiepin

HRID 903653

反応式

HRID 903653 の反応式
[OH-:1].[Na+].C[O:4][C:5]1[CH:21]=[CH:20][C:8]2[S:9][C:10]3[CH:17]=[CH:16][CH:15]=[C:14]([C:18]#N)[C:11]=3[CH2:12][CH2:13][C:7]=2[CH:6]=1.[OH2:22]>C(O)COCCO>[OH:4][C:5]1[CH:21]=[CH:20][C:8]2[S:9][C:10]3[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([OH:22])=[O:1])[C:11]=3[CH2:12][CH2:13][C:7]=2[CH:6]=1

参加物

5

反応条件

温度
200 °C

実験手順

An amount of 2.2 g of sodium hydroxide was dissolved in 30 ml of diethylene glycol by application of heat and to the mixture was added 2.2 g of 2-methoxy-9-cyano-10,11-dihydrodibenzo[b,f]thiepin and the resulting mixture was stirred at 200° C. for 16 hours. After cooling, to the mixture was added water and the mixture was extracted with ethyl acetate. The aqueous layer was acidified with conc. hydrochloric acid and extracted with ethyl acetate. This extract was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate and freed of the solvent to obtain the residue. This residue was recrystallized from benzene to afford 1.1 g (46%) of 2-hydroxy-9-carboxy-10,11-dihydrodibenzo[b,f]thiepin as brown crystals having a melting point of 210°-211° C.

後処理

  1. temperatureof heat and to the mixture
  2. temperatureAfter cooling, to the mixture
  3. extractionthe mixture was extracted with ethyl acetate
  4. extractionextracted with ethyl acetate
  5. washThis extract was washed with saturated sodium chloride solution
  6. dry with materialdried over anhydrous sodium sulfate
  7. customto obtain the residue
  8. customThis residue was recrystallized from benzene

出典と根拠

ORDレコード
ord-603a21f55369406e860621300fd1d1fb
出典データセット
uspto-grants-1980_10
特許番号
US04228284

関連ノート

読み込み中…