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Nitric Acid → HCID 68986110, 화합물

HRID 1430473
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HRID 1430473 반응식
[N+:1]([O-:4])(O)=[O:2].[Br:5][C:6]1[CH:11]=[C:10]([F:12])[CH:9]=[CH:8][C:7]=1[CH2:13][C:14]([OH:16])=[O:15]>>[Br:5][C:6]1[CH:11]=[C:10]([F:12])[C:9]([N+:1]([O-:4])=[O:2])=[CH:8][C:7]=1[CH2:13][C:14]([OH:16])=[O:15]
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참가 물질

3

반응물 2

HCID 944Nitric AcidHCID 34778092-Bromo-4-fluorophenylacetic acid

생성물 1

HCID 68986110HCID 68986110, 화합물수율 92%

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온도
5 °C

실험 절차

Nitric acid (16.00 mL, 322 mmol) was cooled to −15° C. and treated portion-wise with 2-bromo-4-fluorophenylacetic acid (10.00 g, 42.9 mmol) maintaining an internal temperature of −10° C. to −5° C. Once the addition was complete the mixture was warmed to 5° C. over −15 minutes, poured onto ice (200 mL), stirred vigorously until all of the ice melted, and then filtered and rinsed with water. The resulting solid was dissolved in EtOAc, washed with brine, dried (MgSO4) and concentrated to dryness to afford 2-(2-bromo-4-fluoro-5-nitrophenyl)acetic acid (10.93 g, 92% yield) as a bright yellow solid. 1H NMR (400 MHz, DMSO-d6): δ 8.29 (d, 1H), 8.04 (d, 1H), 3.85 (s, 2H).

후처리

  1. temperaturemaintaining an internal temperature of −10° C. to −5° C
  2. additionOnce the addition
  3. additionpoured onto ice (200 mL)
  4. filtrationfiltered
  5. washrinsed with water
  6. dissolutionThe resulting solid was dissolved in EtOAc
  7. washwashed with brine
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated to dryness

출처 및 근거

ORD 기록
ord-58a11badd8bc4f08890766da0bf72d68
출처 데이터셋
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08940756B2

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