Hydrochloric Acid → 1-(Benzo[b]thiophen-4-yl)propan-1-one

HRID 2183614노트

반응식

HRID 2183614 반응식
[S:1]1[CH:5]=[CH:4][C:3]2[C:6]([C:10]#N)=[CH:7][CH:8]=[CH:9][C:2]1=2.[CH2:12]([Mg]Cl)[CH3:13].Cl.CC[O:19]CC>>[S:1]1[CH:5]=[CH:4][C:3]2[C:6]([C:10](=[O:19])[CH2:12][CH3:13])=[CH:7][CH:8]=[CH:9][C:2]1=2

참가 물질

5

반응물 4

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 218165751-Benzothiophene-4-carbonitrileHCID 178461633HCID 178461633, 화합물

생성물 1

HCID 224739661-(Benzo[b]thiophen-4-yl)propan-1-one

실험 절차

A solution of benzo[b]thiophene-4-carbonitrile (24.2 g) in ether (200 ml) was added under nitrogen over 10 minutes to ethylmagnesium chloride (2M solution in ether; 250 ml), then the stirred mixture was heated under reflux for 1 hour, cooled to ambient temperature and poured into crushed ice (100 ml). The mixture was stirred for 30 minutes, then 5M hydrochloric acid (250 ml) was added. The acidic layer was separated, heated to 90° C. for 20 minutes, then allowed to cool to ambient temperature. The product was extracted into ether (500+250 ml), the combined extracts were washed with water (250 ml) and saturated aqueous sodium chloride solution (150 ml), then they were dried (MgSO4) and the solvent was removed in vacuo to give 1-(benzo[b]thiophen-4-yl)propan-1-one (18.25 g) as a colourless oil which was used without further purification.

후처리

  1. temperaturethe stirred mixture was heated
  2. temperatureunder reflux for 1 hour
  3. additionpoured
  4. customThe acidic layer was separated
  5. temperatureheated to 90° C. for 20 minutes
  6. temperatureto cool to ambient temperature
  7. extractionThe product was extracted into ether (500+250 ml)
  8. washthe combined extracts were washed with water (250 ml) and saturated aqueous sodium chloride solution (150 ml)
  9. dry with materialthey were dried (MgSO4)
  10. customthe solvent was removed in vacuo

출처 및 근거

ORD 기록
ord-e6baefabfe2a4096b7ec5fa47792991a
출처 데이터셋
uspto-grants-2005_05
특허 번호
US06900216B2

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