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

Water → HCID 20155091, 화합물

HRID 364920
노트
인쇄 미리보기

반응식

HRID 364920 반응식
[Cl-].[NH4+].O.[CH3:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH2:16][CH:15]([C:17]3[CH:22]=[CH:21][C:20]([N+:23]([O-])=O)=[CH:19][CH:18]=3)[N:14]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[N:13]=2)=[CH:8][CH:7]=1>[Fe].C(O)(=O)C>[NH2:23][C:20]1[CH:21]=[CH:22][C:17]([CH:15]2[N:14]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[N:13]=[C:12]([C:9]3[CH:8]=[CH:7][C:6]([O:5][CH3:4])=[CH:11][CH:10]=3)[CH2:16]2)=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 44365033-(4-Methoxyphenyl)-5-(4-nitrophenyl)-1-phenyl-2-pyrazoline

생성물 1

HCID 20155091HCID 20155091, 화합물수율 80.5%

시약·촉매·용매 2

HCID 23925Iron촉매HCID 176Acetic Acid용매

실험 절차

15.8 g of metallic iron powder and 1.6 g of ammonium chloride were dispersed in a mixed solution of 140 ml of iospropyl alcohol and 14 ml of water, and, while stirring and refluxing under heating, 13.1 g of 3-(4-methoxyphenyl)-5-(4-nitrophenyl)-1-phenyl-2-pyrazoline was added thereto. After refluxing for 2 hours, 10 ml of acetic acid was added thereto, and the reaction was thereafter continued for 30 minutes under refluxing. Solids were removed by filtration using sellaite, and 150 ml of water was added to the filtrate. Crystals precipitated were collected by filtration to obtain 9.7 g of 5-(4-aminophenyl)-3-(4-methoxyphenyl)-1-phenyl-2-pyrazoline. m.p. 164°-166° C.

후처리

  1. temperaturerefluxing
  2. temperatureunder heating
  3. temperatureAfter refluxing for 2 hours
  4. temperatureunder refluxing
  5. customSolids were removed by filtration
  6. additionwas added to the filtrate
  7. customCrystals precipitated
  8. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-d909a80332484beeb01e4d9f205cd1fd
출처 데이터셋
uspto-grants-1986_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04607006

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트