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Hydrazine hydrate (1:1) → HCID 15754479, 화합물

HRID 1030011
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반응식

HRID 1030011 반응식
[N+:1]([C:4]1[CH:19]=[CH:18][CH:17]=[CH:16][C:5]=1[C:6]([CH:8]1[C:13](=O)[CH2:12][CH2:11][CH2:10][C:9]1=[O:15])=O)([O-:3])=[O:2].O.[NH2:21][NH2:22]>C(O)C>[O:15]=[C:9]1[CH2:10][CH2:11][CH2:12][C:13]2[NH:22][N:21]=[C:6]([C:5]3[CH:16]=[CH:17][CH:18]=[CH:19][C:4]=3[N+:1]([O-:3])=[O:2])[C:8]1=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 139830702-(2-Nitrobenzoyl)cyclohexane-1,3-dione

생성물 1

HCID 15754479HCID 15754479, 화합물수율 45%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

3.2 g (12.2 mmol) of 2-nitrobenzoylcyclohexane-1,3-dione and 0.52 g (12.2 mmol) of hydrazine hydrate (80%) are refluxed for 4 hours in 120 ml of ethanol. The ethanol is subsequently distilled off under reduced pressure, and 80 ml of methanol are added. The solid which precipitates is filtered off with suction and dried in vacuo. 1.41 g (45% of theory) of 4,5,6,7-tetrahydro-4-oxo-3-(2-nitro-phenyl)-1H-indazole of the formula ##STR6## and of melting point 236° C. (decomp.) are obtained.

후처리

  1. distillationThe ethanol is subsequently distilled off under reduced pressure, and 80 ml of methanol
  2. additionare added
  3. customThe solid which precipitates
  4. filtrationis filtered off with suction
  5. customdried in vacuo

출처 및 근거

ORD 기록
ord-a5128ff284f84dac861cca4460a0f13f
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05104442

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