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4-Amino-3-nitrophenyl thiocyanate → 1-(3-Methoxycarbonyl-2-thioureido)-2-nitro-4-thiocyanatobenzene

HRID 616084
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인쇄 미리보기

반응식

HRID 616084 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]#[N:10])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12].[CH3:14][O:15][C:16]([N:18]=[C:19]=[S:20])=[O:17]>CC(C)=O>[CH3:14][O:15][C:16]([NH:18][C:19](=[S:20])[NH:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]#[N:10])=[CH:4][C:3]=1[N+:11]([O-:13])=[O:12])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1046774-Amino-3-nitrophenyl thiocyanateHCID 552246Methoxycarbonyl isothiocyanate

생성물 1

HCID 203710751-(3-Methoxycarbonyl-2-thioureido)-2-nitro-4-thiocyanatobenzene

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

2.0 G. of 1-amino-2-nitro-4-thiocyanatobenzene in 20 ml. acetone is treated with 3.0 g. methoxycarbonyl isothiocyanate at room temperature for 9 days. The solution is concentrated and the residue triturated with methanol and recrystallized from acetone, yielding 1-(3-methoxycarbonyl-2-thioureido)- 2-nitro-4-thiocyanatobenzene.

후처리

  1. concentrationThe solution is concentrated
  2. customthe residue triturated with methanol
  3. customrecrystallized from acetone

출처 및 근거

ORD 기록
ord-5b12b509635948e0ad99edc16eebb117
출처 데이터셋
uspto-grants-1978_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04072696

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