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Hydrazine hydrate (1:1) → HCID 85873980, 화합물

HRID 866920
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인쇄 미리보기

반응식

HRID 866920 반응식
[C:1]([C:3]1[C:8]2[CH2:9][C:10](=O)[C:11]3[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=3[S:13][C:7]=2[CH:6]=[CH:5][CH:4]=1)#[N:2].O.[NH2:20][NH2:21]>C(O)C>[C:1]([C:3]1[C:8]2[CH2:9][C:10](=[N:20][NH2:21])[C:11]3[CH:17]=[CH:16][CH:15]=[CH:14][C:12]=3[S:13][C:7]=2[CH:6]=[CH:5][CH:4]=1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 126870859-Cyano 10,11-dihydro-11-oxo-dibenzo[b,f]thiepin

생성물 1

HCID 85873980HCID 85873980, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

0.9g of 9-cyano-10,11-dihydro-11-oxo-dibenzo[b,f]thiepin and 1g of 100% hydrazine hydrate were dissolved in 10ml of ethanol and the resulting mixture was heated under reflux for 3.5 hours. The reaction mixutre was concentrated to 5ml to separate crystals on cooling, which were collected by filtration. Recrystallization from ethanol afforded 0.6g of 9-cyano-10,11-dihydro-11-oxo-dibenzo-[b,f]thiepin hydrazone as pale brown prismatic crystals having a melting point of 175°-177° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperaturethe resulting mixture was heated
  2. temperatureunder reflux for 3.5 hours
  3. concentrationThe reaction mixutre was concentrated to 5ml
  4. customto separate crystals
  5. temperatureon cooling
  6. filtrationwhich were collected by filtration
  7. customRecrystallization from ethanol

출처 및 근거

ORD 기록
ord-55993361452048f09fbe6cc7496394a0
출처 데이터셋
uspto-grants-1978_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04101667

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