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Hydrochloric Acid → 1-(3-Thienyl)-2-propen-1-one

HRID 2179972
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HRID 2179972 반응식
CON(C)[C:4]([C:6]1[CH:10]=[CH:9][S:8][CH:7]=1)=[O:5].[CH:12]([Mg]Br)=[CH2:13].Cl>O1CCCC1>[S:8]1[CH:9]=[CH:10][C:6]([C:4](=[O:5])[CH:12]=[CH2:13])=[CH:7]1
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 22489894N-methoxy-N-methylthiophene-3-carboxamideHCID 178418507HCID 178418507, 화합물

생성물 1

HCID 224899271-(3-Thienyl)-2-propen-1-one수율 77%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-10 °C

실험 절차

The product from step (a) (2.074 g, 12.1 mmol) was dissolved in anhydrous tetrahydrofuran (30 ml) and the solution cooled to −10° C. Vinyl magnesium bromide (1M, 14.5 ml, 14.5 mmol) was added dropwise, keeping the temperature below 0° C. The resultant solution was stirred at 0° C. for 2.5 h, then allowed to warm to room temperature. The reaction mixture was slowly poured into aqueous 2M hydrochloric acid (200 ml) and ice. Extracted with ethyl acetate (3×70 ml) and the combined extracts were washed with water (2×30 ml) and brine (20 ml), dried (magnesium sulphate) and evaporated in vacuo to give the title compound (1.288 g, 77%).

후처리

  1. customthe temperature below 0° C
  2. temperatureto warm to room temperature
  3. extractionExtracted with ethyl acetate (3×70 ml)
  4. washthe combined extracts were washed with water (2×30 ml) and brine (20 ml)
  5. dry with materialdried (magnesium sulphate)
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-60b53abd57254ee0840b2d439c7eef2c
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06887871B2

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