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Water → 2-bromo-4-nitro-6-(trifluoromethyl)aniline

HRID 1783344
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HRID 1783344 반응식
[Br:1]Br.[N+:3]([C:6]1[CH:11]=[CH:10][C:9]([NH2:12])=[C:8]([C:13]([F:16])([F:15])[F:14])[CH:7]=1)([O-:5])=[O:4].O>C(O)(=O)C>[Br:1][C:10]1[CH:11]=[C:6]([N+:3]([O-:5])=[O:4])[CH:7]=[C:8]([C:13]([F:14])([F:15])[F:16])[C:9]=1[NH2:12]
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참가 물질

5

반응물 3

HCID 962WaterHCID 24408BromineHCID 671284-Nitro-alpha,alpha,alpha-trifluoro-o-toluidine

생성물 1

HCID 114716542-bromo-4-nitro-6-(trifluoromethyl)aniline수율 91%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

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온도
120 °C

실험 절차

Bromine (0.60 mL) dissolved in acetic acid (11 mL) was added dropwise to a solution of 4-nitro-2-trifluoromethyl-phenylamine (2.4 g) in acetic acid (12 mL). The reaction mixture was heated to 120° C. for 2½ hours, poured into water (400 mL) and filtered. The collected solid was washed with water (200 mL) and dried in vacuo to furnish 3.03 g (91% yield) of the title compound as a yellow solid. 1H NMR (500 MHz, DMSO-d6): 7.08 (s, 2H), 8.23 (d, 1H), 8.51 (d, 1H).

후처리

  1. filtrationfiltered
  2. washThe collected solid was washed with water (200 mL)
  3. customdried in vacuo

출처 및 근거

ORD 기록
ord-eb0397acdf094dd49207fab7ba10a240
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501414B2

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