홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

tert-Butyl carbazate → Tert-butyl 2-(3-cyanobenzylidene)-1-hydrazinecarboxylate

HRID 1181188
노트
인쇄 미리보기

반응식

HRID 1181188 반응식
[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=O)#[N:2].[C:11]([O:15][C:16](=[O:19])[NH:17][NH2:18])([CH3:14])([CH3:13])[CH3:12]>CCO>[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH:6]=[N:18][NH:17][C:16]([O:15][C:11]([CH3:14])([CH3:13])[CH3:12])=[O:19])#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 70091tert-Butyl carbazateHCID 90670m-Formylbenzonitrile

생성물 1

HCID 69314844Tert-butyl 2-(3-cyanobenzylidene)-1-hydrazinecarboxylate수율 77%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

3-Cyanobenzaldehyde (40.0 mmol) suspended in EtOH (100 mL) was added to a stirred solution of tert-butylcarbazate (40.0 mmol) in EtOH. The mixture was heated at reflux temperature and after 4 h the EtOH was partially evaporated in vacuo. Water (100 mL) was added and the precipitated product was collected by filtration and washed with diethylether to give tert-butyl 2-(3-cyanobenzylidene)-1-hydrazinecarboxylate as a white solid.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux temperature
  3. customafter 4 h the EtOH was partially evaporated in vacuo
  4. additionWater (100 mL) was added
  5. filtrationthe precipitated product was collected by filtration
  6. washwashed with diethylether

출처 및 근거

ORD 기록
ord-d57f2d9fe43d421ca4219b3e149b9522
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07285547B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트