Hydrochloric Acid → 4,5,6,7-Tetrahydro-7-oxobenzo[b]thiophen-4-amine hydrochloride

HRID 263203노트

반응식

HRID 263203 반응식
[O:1]=[C:2]1[C:7]2[S:8][CH:9]=[CH:10][C:6]=2[CH:5]([NH:11]C=O)[CH2:4][CH2:3]1.[ClH:14]>C(O)C>[ClH:14].[O:1]=[C:2]1[C:7]2[S:8][CH:9]=[CH:10][C:6]=2[CH:5]([NH2:11])[CH2:4][CH2:3]1

참가 물질

4

실험 절차

A mixture of (+)-N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)formamide (52.65 grams) in 525 ml. of 95% ethanol and 525 ml. of 2 N HCl is heated at reflux for two hours. The mixture is cooled, filtered through glass wool and the filtrate is evaporated to dryness. The dark solid is dissolved in 180 ml. of water and the insoluble material is collected by filtration. The filter cake is washed with 70 ml. of water and the combined solution containing the title compound is used in the next operation. A 3 ml. solution is evaporated to dryness and the residue is dissolved in 95% ethanol. The ethanol solution is decolorized with activated carbon and filtered. The filtrate is evaporated to dryness to afford 0.5 grams of the title compound, m.p. 212°-214° C. (dec.), [α]D26 =+13.56° (c, 0.59 in methanol).

후처리

  1. temperatureat reflux for two hours
  2. temperatureThe mixture is cooled
  3. filtrationfiltered through glass wool
  4. customthe filtrate is evaporated to dryness
  5. dissolutionThe dark solid is dissolved in 180 ml
  6. filtrationof water and the insoluble material is collected by filtration
  7. washThe filter cake is washed with 70 ml
  8. additionof water and the combined solution containing the title compound
  9. customsolution is evaporated to dryness
  10. dissolutionthe residue is dissolved in 95% ethanol
  11. filtrationfiltered
  12. customThe filtrate is evaporated to dryness

출처 및 근거

ORD 기록
ord-5ac22b3d044a42fc9cc798c165f4ebab
출처 데이터셋
uspto-grants-1979_05
특허 번호
US04156670

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