Diethyl Ether → Dibenzyl 5-aminoisophthalate

HRID 889841노트

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HRID 889841 반응식
[CH2:1]([O:8][C:9](=[O:29])[C:10]1[CH:25]=[C:24]([N+:26]([O-])=O)[CH:23]=[C:12]([C:13]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:14])[CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CCOCC>C(O)(=O)C.[Zn]>[CH2:16]([O:15][C:13](=[O:14])[C:12]1[CH:23]=[C:24]([NH2:26])[CH:25]=[C:10]([C:9]([O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[O:29])[CH:11]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

참가 물질

5

실험 절차

In acetic acid (15 mL) was stirred 5-nitroisophthalic acid dibenzyl ester (1.3 g, 3.3 mmol). To this was added in parts zinc dust (1.75 g, 26.6 mmol). The mixture was stirred at room temperature for 18 hours. The mixture was filtered free of insoluble material and the acetic acid solution evaporated at reduced pressure. This residue was dissolved in ethyl acetate (120 mL) and washed successively with saturated sodium bicarbonate solution (50 mL), water (50 mL), and brine (50 mL). The organic phase was dried over magnesium sulfate and evaporated in vacuo to give a solid. The solid was stirred into ether (75 mL) and brought to reflux. The solution allowed to recrystallize to give 260 mg (22%) of a white solid. MS: M+1=362.2.

후처리

  1. filtrationThe mixture was filtered free of insoluble material
  2. customthe acetic acid solution evaporated at reduced pressure
  3. dissolutionThis residue was dissolved in ethyl acetate (120 mL)
  4. washwashed successively with saturated sodium bicarbonate solution (50 mL), water (50 mL), and brine (50 mL)
  5. dry with materialThe organic phase was dried over magnesium sulfate
  6. customevaporated in vacuo
  7. customto give a solid
  8. temperatureto reflux
  9. customto recrystallize

출처 및 근거

ORD 기록
ord-733def17de0f4c6ea64fa843d7cb3d57
출처 데이터셋
uspto-grants-2006_02
특허 번호
US06995151B2

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