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HCID 68890072, 화합물 → 2-(4-bromo-2-fluorophenyl)ethanamine

HRID 988973
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HRID 988973 반응식
[Br:1][C:2]1[CH:12]=[CH:11][C:5]([CH:6]=[CH:7][N+:8]([O-])=O)=[C:4]([F:13])[CH:3]=1>C1COCC1>[Br:1][C:2]1[CH:12]=[CH:11][C:5]([CH2:6][CH2:7][NH2:8])=[C:4]([F:13])[CH:3]=1
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참가 물질

3

반응물 1

HCID 68890072HCID 68890072, 화합물

생성물 1

HCID 222508972-(4-bromo-2-fluorophenyl)ethanamine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
0 °C

실험 절차

4-Bromo-2-fluoronitro styrene (1 equivalent) in THF (0.2 M) was cooled to 0° C. and treated with 1.0 M BH3 in THF (5 equivalents). The reaction was heated to reflux overnight. The reaction was cooled to 0° C. and quenched with H2O then 1 N HCl until a pH of about 2 was achieved. The reaction was stirred for 30 minutes at room temperature and then extracted with ether (3×). The aqueous layer was made basic with 5% NaOH solution. The aqueous layer was then extracted into ether (3×). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated to give crude 2-(4-bromo-2-fluorophenyl)ethylamine. Purification by flash chromatography eluting with 2%-5%-10% MeOH/CH2Cl2 gradients containing 1% concentrated ammonia afforded the desired compound. MS m/z 219.8 (M+H).

후처리

  1. additiontreated with 1.0 M
  2. temperatureThe reaction was heated
  3. temperatureto reflux overnight
  4. customquenched with H2O
  5. extractionextracted with ether (3×)
  6. extractionThe aqueous layer was then extracted into ether (3×)
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customto give crude 2-(4-bromo-2-fluorophenyl)ethylamine
  12. customPurification by flash chromatography
  13. washeluting with 2%-5%-10% MeOH/CH2Cl2 gradients
  14. additioncontaining 1% concentrated ammonia

출처 및 근거

ORD 기록
ord-f0d6c0cd51ce4d1fa940505cdb2469dc
출처 데이터셋
uspto-grants-2003_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06638927B2

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