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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Succinic anhydride → HCID 59324177, 화합물

HRID 538751
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인쇄 미리보기

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HRID 538751 반응식
[F:1][C:2]([F:8])([F:7])[C:3]1([NH2:6])[CH2:5][CH2:4]1.C(N(C(C)C)CC)(C)C.[C:18]1(=[O:24])[O:23][C:21](=[O:22])[CH2:20][CH2:19]1>O1CCOCC1>[O:24]=[C:18]([NH:6][C:3]1([C:2]([F:8])([F:7])[F:1])[CH2:5][CH2:4]1)[CH2:19][CH2:20][C:21]([OH:23])=[O:22]
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참가 물질

5

반응물 3

HCID 7922Succinic anhydrideHCID 81531DiisopropylethylamineHCID 116511971-(Trifluoromethyl)cyclopropanamine

생성물 1

HCID 59324177HCID 59324177, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
10 °C

실험 절차

Slowly, 800.7 mg (4.96 mmol) of 1-(trifluoromethyl)cyclopropanamine and 0.85 ml (4.96 mmol) of diisopropylethylamine were added to a solution of 496 mg (4.96 mmol) of succinic anhydride in 10 ml of dioxane, with ice-cooling (10° C.). Stirring was continued for 20 min at room temperature, and the mixture was allowed to stand overnight at this temperature. Again, stirring was continued for 20 min at 80° C., the mixture was allowed to cool to room temperature, and the solution was concentrated. Repeatedly, the solution was washed alternately with ethyl acetate and with water. The combined organic phases were dried and concentrated. This gave 815.8 mg (73% of theory) of the desired compound.

후처리

  1. waitto stand overnight at this temperature
  2. stirringAgain, stirring
  3. waitwas continued for 20 min at 80° C.
  4. temperatureto cool to room temperature
  5. concentrationthe solution was concentrated
  6. washRepeatedly, the solution was washed alternately with ethyl acetate and with water
  7. customThe combined organic phases were dried
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ef070a10fb394478a79d2a4429c3ae54
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08865759B2

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