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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetone → ST001233

HRID 1774292
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반응식

HRID 1774292 반응식
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][C:10]([CH3:12])=O.[C:13](#[N:17])[CH2:14][C:15]#[N:16].C([O-])(=O)C.[NH4+:22]>>[NH2:16][C:15]1[N:22]=[C:10]([CH3:12])[CH:9]=[C:1]([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[C:14]=1[C:13]#[N:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 180AcetoneHCID 240BenzaldehydeHCID 8010MalononitrileHCID 517165Ammonium Acetate

생성물 1

HCID 610514ST001233수율 40%

실험 절차

Benzaldehyde (406 μl, 4 mmol), acetone (294 μl, 4 mmol), malononitrile (264 mg, 4 mmol) e ammonium acetate (462 mg, 6 mmol) were placed in a microwave tube and irradiated with microwaves (Solvent: none; Power: 150 W; Ramp time: 5 min; Heating time: 10 min; Temperature: 100° C.; Pressure: 175 psi; Stirring: on; Cooling: on). At the end of the microwave irradiation cycle, the solvent was removed under reduced pressure. The crude product was purified by flash chromatography on silica gel (petroleum ether/ethyl acetate=90/10) to obtain 2-amino-4-phenyl-6-methylnicotinonitrile in 40% yield.

후처리

  1. customirradiated with microwaves (Solvent: none; Power: 150 W; Ramp time: 5 min; Heating time: 10 min; Temperature: 100° C.; Pressure: 175 psi; Stirring: on; Cooling: on)
  2. customAt the end of the microwave irradiation cycle
  3. customthe solvent was removed under reduced pressure
  4. customThe crude product was purified by flash chromatography on silica gel (petroleum ether/ethyl acetate=90/10)

출처 및 근거

ORD 기록
ord-745ca3445bb7414c8101155f63f43a98
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09260394B2

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