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Dibenzylamine → HCID 23454956, 화합물

HRID 1680895
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HRID 1680895 반응식
[CH2:1]([NH:8][CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:16]([NH:18][NH:19][C:20]1[CH:25]=[CH:24][C:23]([N:26]=[C:27]=[S:28])=[CH:22][CH:21]=1)=[O:17]>C(O)C>[CH:16]([NH:18][NH:19][C:20]1[CH:25]=[CH:24][C:23]([NH:26][C:27]([N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[S:28])=[CH:22][CH:21]=1)=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7656DibenzylamineHCID 20283022N'-(4-Isothiocyanatophenyl)formohydrazide

생성물 1

HCID 23454956HCID 23454956, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Dibenzylamine (0.20 g, 0.001 mole) and 4-(2-formylhydrazino)phenyl isothiocyanate (0.19 g, 0.001 mole) were mixed in ethanol (25 ml) and the resulting mixture was heated to reflux for 20 minutes. The reaction mixture was cooled to room temperature, then was chilled in ice. After scratching the flask walls, a white crystalline solid was separated out of solution. The solid was filtered off, washed thoroughly with ether, and allowed to dry. This gave 0.31 g (80 percent) of product as a white crystalline powder, m.p. 174°-176° C.

후처리

  1. temperaturethe resulting mixture was heated
  2. temperatureto reflux for 20 minutes
  3. temperaturewas chilled in ice
  4. customa white crystalline solid was separated out of solution
  5. filtrationThe solid was filtered off
  6. washwashed thoroughly with ether
  7. customto dry

출처 및 근거

ORD 기록
ord-1f594226463a4f0895c788e4ddef76de
출처 데이터셋
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04276364

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