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Hydrochloric Acid → 2-Chloro-5-fluoro-4-methoxyaniline

HRID 1831489
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HRID 1831489 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([F:10])=[CH:4][C:3]=1[N+:11]([O-])=O.Cl>O>[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[C:5]([F:10])=[CH:4][C:3]=1[NH2:11]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 220520461-Chloro-4-fluoro-5-methoxy-2-nitrobenzene

생성물 1

HCID 220520702-Chloro-5-fluoro-4-methoxyaniline수율 186.7%

시약·촉매·용매 1

HCID 962Water용매

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온도
55 °C

실험 절차

1-Chloro-4-fluoro-5-methoxy-2-nitro-benzene (16.3 g, 79.3 mmol) and Sn granules (29.1 g, 246 mmol) were suspended in water (200 mL). Concentrated HCl (79 mL, 952 mmol) was added dropwise over 20 min. The resulting mixture was heated to 55° C. for 3 h. The solution was cooled to room temperature and carefully quenched with 1 N NaOH. The thick mixture was filtered through celite eluting the ethyl acetate to give a clear solution which was extracted with ethyl acetate. The ethyl acetate layers were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo to give 26 g (80%) of 2-chloro-5-fluoro-4-methoxyaniline: Crude 1H NMR (400 MHz, CDCl3): δ 6.88 (d, J=8.3 Hz, 1H), 6.57 (d, J=12.2 Hz, 1H), 3.79 (s, 3H), 3.77 (br s, 2H). The crude material was pure enough to carry on to the next step.

후처리

  1. temperatureThe solution was cooled to room temperature
  2. customcarefully quenched with 1 N NaOH
  3. filtrationThe thick mixture was filtered through celite
  4. washeluting the ethyl acetate
  5. customto give a clear solution which
  6. extractionwas extracted with ethyl acetate
  7. washThe ethyl acetate layers were washed with brine
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-be493efc37c44551aee5efabc7654a20
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07067658B2

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