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Ethylamine → N-Ethyl-3-nitro PABA

HRID 1591968
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HRID 1591968 반응식
F[C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[CH2:14]([NH2:16])[CH3:15]>CO>[CH2:14]([NH:16][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12])[CH3:15]
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참가 물질

4

반응물 2

HCID 6341EthylamineHCID 679874-Fluoro-3-nitrobenzoic acid

생성물 1

HCID 3729086N-Ethyl-3-nitro PABA

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
75 °C

실험 절차

To a suspension of 1.85 g of 4-fluoro-3-nitrobenzoic acid (10 mmol) in 25 mL of MeOH is added 20 mL of ethylamine (2.0M in THF). The resulting yellow solution is stirred at 75° C. for 5 h then at RT for 48 h. The solvent is removed under reduced pressure, then water is added to the residue. The resulting orange suspension is acidified with 2N aqueous HCl and the yellow precipitate is collected by filtration, washed with water and dried in vacuo to give 4-ethylamino-3-nitro-benzoic acid: mp=233-236° C.; 1H-NMR (DMSO-d6) δ 12.83 (s, 1H), 8.61 (d, J=1.84, 1H), 8.49 (m, 1H), 7.97 (dd, 1H), 7.12 (d, J=9.2, 1H), 3.46 (m, 2H), 1.23 (t, 3H); [M−1]−=209.

후처리

  1. waitat RT for 48 h
  2. customThe solvent is removed under reduced pressure
  3. additionwater is added to the residue
  4. filtrationthe yellow precipitate is collected by filtration
  5. washwashed with water
  6. customdried in vacuo

출처 및 근거

ORD 기록
ord-5df5124fc50746d2b05e96d8c798951b
출처 데이터셋
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07291635B2

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