(4-Nitrophenyl)acetic acid → 2-(4-Nitrophenyl)acetohydrazide

HRID 1921622

반응식

HRID 1921622 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([OH:13])=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].C(Cl)(=O)C(Cl)=O.CN(C=O)C.[NH2:25][NH2:26]>ClCCl>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH2:10][C:11]([NH:25][NH2:26])=[O:13])=[CH:6][CH:5]=1)([O-:3])=[O:2]

참가 물질

6

반응물 4

HCID 4661(4-Nitrophenyl)acetic acidHCID 6228DimethylformamideHCID 9321HydrazineHCID 65578Oxalyl chloride

생성물 1

HCID 2873312-(4-Nitrophenyl)acetohydrazide

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of 4-nitrophenylacetic acid (2.81 mmol) in dry dichloromethane (10 mL) was treated with a 2N solution of oxalyl chloride (3.0 mL) and DMF (0.02 mL) via syringe, and the reaction stirred at ambient temperature for 1 h. The reaction was concentrated to dryness in vacuo and the crude product was dissolved in dry dichloro-methane (20 mL), treated with anhydrous hydrazine (11.1 mmol) via syringe, and stirred at ambient temperature for 18 h. The resulting suspension was filtered, solids rinsed with dichloromethane, dissolved in MeOH/CH2Cl2, filtered, and filtrate concentrated in vacuo giving the title compound as an orange solid. 1H NMR (DMSO-d6) δ 8.17 (2H, d, J=8.8 Hz,), 7.54 (2H, d, J=8.8 Hz), 3.54 (2H, s).

후처리

  1. concentrationThe reaction was concentrated to dryness in vacuo
  2. dissolutionthe crude product was dissolved in dry dichloro-methane (20 mL)
  3. stirringstirred at ambient temperature for 18 h
  4. filtrationThe resulting suspension was filtered
  5. washsolids rinsed with dichloromethane
  6. dissolutiondissolved in MeOH/CH2Cl2
  7. filtrationfiltered
  8. concentrationfiltrate concentrated in vacuo

출처 및 근거

ORD 기록
ord-0db6b45f70844e0e9f4000e1585658c0
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08173654B2

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