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Ammonia → C-(2,4-Dimethoxyphenyl)-C-(2-methoxyphenyl)methylamine

HRID 19714
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HRID 19714 반응식
[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][C:4]=1[C:5](=[N:14]O)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[O:12][CH3:13].N.C([O-])(=O)C.[NH4+]>C(O)C.C(OCC)(=O)C.[Zn]>[CH3:1][O:2][C:3]1[CH:19]=[C:18]([O:20][CH3:21])[CH:17]=[CH:16][C:4]=1[CH:5]([NH2:14])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[O:12][CH3:13]
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참가 물질

7

반응물 3

HCID 222AmmoniaHCID 517165Ammonium AcetateHCID 86611440HCID 86611440, 화합물

생성물 1

HCID 43197268C-(2,4-Dimethoxyphenyl)-C-(2-methoxyphenyl)methylamine

시약·촉매·용매 3

HCID 23994Zinc촉매HCID 702Ethanol용매
HCID 8857
Ethyl Acetate
용매

실험 절차

2,2′,4-Trimethoxybenzophenone oxime (6 g, 20.9 mmol) is dissolved in ethanol (30 ml) and concentrated aqueous ammonia (150 ml). Ammonium acetate (0.81 g, 10.45 mmol) is added, followed by zinc powder (6.79 g, 104 mmol). The reaction is heated to reflux for 4 hours, cooled to ambient temperature, diluted with ethyl acetate and filtered through a Celite™ filter. Evaporation affords the title compound. δH 3.78 (s 3H), 3.80 (s 3H), 3.82 (s 3H), 5.62 (s 3H), 6.40-6.50 (m 2H), 6.85-9.95 (m 2H), 7.10 (d J 8), 7.20-7.30 (m 2H)

후처리

  1. temperatureThe reaction is heated
  2. temperatureto reflux for 4 hours
  3. filtrationfiltered through a Celite™
  4. filtrationfilter
  5. customEvaporation

출처 및 근거

ORD 기록
ord-d086c88d01994e01b7fbf7faf0ac7880
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07745462B2

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