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Ethyl 4,4,4-trifluoroacetoacetate → CID 90109439

HRID 1508936
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HRID 1508936 반응식
[CH:1]1([C:6](=[NH:8])[NH2:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.[F:9][C:10]([F:20])([F:19])[C:11](=O)[CH2:12][C:13](OCC)=[O:14].C[O-].[Na+]>C(O)C>[CH:1]1([C:6]2[N:7]=[C:13]([OH:14])[CH:12]=[C:11]([C:10]([F:20])([F:19])[F:9])[N:8]=2)[CH2:5][CH2:4][CH2:3][CH2:2]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 67793Ethyl 4,4,4-trifluoroacetoacetateHCID 4452694CyclopentanecarboximidamideHCID 10942334Sodium Methoxide

생성물 1

HCID 178516140CID 90109439수율 36%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
85 °C

실험 절차

To a solution of cyclopentanecarboximidamide (3.0 g, 27.1 mmol) in ethanol (100 mL) was added ethyl 4,4,4-trifluoro-3-oxobutanoate (5.0 g, 27.1 mmol) and sodium methoxide (1.76 g, 32.5 mmol). The mixture was stirred at 85° C. for 16 h. After this time, the mixture was concentrated, diluted with ethanol (10 mL), and the suspension was chilled to 0° C. HCl (2M, 50 mL) was added and the suspension was filtered and washed with water. The solid was dried under heat and vacuum to afford the title compound (2.24 g, 36%) as a white solid. MW=232.20. 1H NMR (DMSO-d6, 500 MHz) δ 12.96 (s, 1H), 6.67 (s, 1H), 3.03 (quin, J=8.2 Hz, 1H), 2.00-1.92 (m, 2H), 1.83-1.67 (m, 4H), 1.64-1.53 (m, 2H); APCI MS m/z 233 [M+H]+.

후처리

  1. concentrationAfter this time, the mixture was concentrated
  2. additiondiluted with ethanol (10 mL)
  3. temperaturethe suspension was chilled to 0° C
  4. additionHCl (2M, 50 mL) was added
  5. filtrationthe suspension was filtered
  6. washwashed with water
  7. customThe solid was dried
  8. temperatureunder heat

출처 및 근거

ORD 기록
ord-7c18efbbe44b4843a10f55b107f3c576
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09221843B2

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