Water → Dibenzo(b,f)thiepin-1-carboxylic acid, 10,11-dihydro-8-methoxy-

HRID 866937ノート

反応式

HRID 866937 の反応式
[OH-:1].[K+].[CH3:3][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)C>[CH3:3][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]([OH:22])=[O:1])[C:11]=3[CH2:12][CH2:13][C:7]=2[CH:6]=1

参加物

5

実験手順

An amount of 6.0g potassium hydroxide was dissolved in 20ml of 80% ethanol and to the solution was added 1g of 2-methoxy-9-cyano-10,11-dihydrodibenzo[b,f]thiepin and the resulting mixture was refluxed for 26 hours. The mixture was freed of the solvent under reduced pressure to obtain the residue, which was dissolved in water and extracted with ethyl acetate. The aqueous layer was acidified with conc. hydrochloric acid and extracted with ethyl acetate. The extract was washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate and freed of the solvent to give 743 mg (69%) of 2-methoxy-9-carboxy-10,11-dihydrodibenzo[b,f]thiepin as pale reddish needles having a melting point of 185°-186° C.

後処理

  1. temperaturethe resulting mixture was refluxed for 26 hours
  2. customto obtain the residue, which
  3. extractionextracted with ethyl acetate
  4. extractionextracted with ethyl acetate
  5. washThe extract was washed with saturated sodium chloride solution
  6. dry with materialdried over anhydrous sodium sulfate

出典と根拠

ORDレコード
ord-78294fe96ff244f2a6ef9ec7869ed128
出典データセット
uspto-grants-1978_07
特許番号
US04101667

反応ノート

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