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Benzenediazonium chloride → 3-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid

HRID 462520
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HRID 462520 반응식
[Na].[OH:2][C:3]1[CH2:4][CH:5]([C:10]([OH:12])=[O:11])[CH2:6][C:7](=[O:9])[CH:8]=1.[Cl-].[C:14]1([N+:20]#[N:21])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>CO>[OH:2][C:3]1[CH2:4][CH:5]([C:10]([OH:12])=[O:11])[CH2:6][C:7](=[O:9])[C:8]=1[N:21]=[N:20][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 60992Benzenediazonium chlorideHCID 5360545SodiumHCID 144923703-Hydroxy-5-oxocyclohex-3-ene-1-carboxylic acid

생성물 1

HCID 1355835033-Hydroxy-5-keto-4-phenylazo-3-cyclohexenecarboxylic acid

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

13.8 g. of sodium were dissolved in 900 ml. of methanol and to this solution were added 46.8 g. of 3-hydroxy-5-keto-3-cyclohexene-carboxylic acid. The resulting mixture was stirred, maintained between -4° C. and -8° C. by means of a cooling bath and treated over a period of 30 minutes with a phenyl-diazonium chloride solution (prepared from 27.9 g. of aniline, 450 ml. of water, 72 ml. of concentrated hydrochloric acid and 21.0 g. of sodium nitrite in 90 ml. of water). The resulting mixture was stirred for an additional hour at -5° C. to -10° C. The precipitated red reaction product was removed by filtration with suction and washed with about 1000 ml. of water, whereby there was obtained 3-hydroxy-5-keto-4-phenylazo-3-cyclohexene-carboxylic acid having a melting point of 218° C.

후처리

  1. temperaturemaintained between -4° C. and -8° C. by means of a cooling bath
  2. stirringThe resulting mixture was stirred for an additional hour at -5° C. to -10° C
  3. customThe precipitated red reaction product was removed by filtration with suction
  4. washwashed with about 1000 ml

출처 및 근거

ORD 기록
ord-1a869e6207ab42dc968061fef556b461
출처 데이터셋
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04515948

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