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Nitric Acid → 4-Chloro-3-nitro-valerophenone

HRID 2058012
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반응식

HRID 2058012 반응식
[Cl:1][CH:2]([CH3:13])[CH2:3][CH2:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6].[N+:14]([O-])([OH:16])=[O:15]>S(=O)(=O)(O)O>[Cl:1][CH:2]([CH3:13])[CH:3]([N+:14]([O-:16])=[O:15])[CH2:4][C:5]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 944Nitric AcidHCID 144729704-Chlorovalerophenone

생성물 1

HCID 205284754-Chloro-3-nitro-valerophenone

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매2회

실험 절차

50 ml of concentrated sulphuric acid are treated, while stirring, with 9.9 g of 4-chloro-valerophenone, while cooling with an ice/sodium chloride mixture. The bulk of the product dissolves, a slightly exothermic reaction taking place, and a yellow suspension forms, which is treated, while stirring vigorously and at a temperature of -10° to -5°, with a mixture of 20 ml of concentrated sulphuric acid and 10.4 ml of concentrated nitric acid (d=1.52), in the course of 10 minutes. After a reaction time of five minutes, the mixture is poured onto ice and the aqueous mixture is extracted with chloroform. The organic extract is washed once with an aqueous solution of sodium carbonate and with water, dried over sodium sulphate and filtered through silica gel. 4-Chloro-3-nitro-valerophenone is obtained as an oily residue after evaporating the filtrate.

후처리

  1. dissolutionThe bulk of the product dissolves
  2. customa slightly exothermic reaction
  3. additiona yellow suspension forms, which is treated
  4. additionAfter a reaction time of five minutes, the mixture is poured onto ice
  5. extractionthe aqueous mixture is extracted with chloroform
  6. extractionThe organic extract
  7. washis washed once with an aqueous solution of sodium carbonate and with water
  8. dry with materialdried over sodium sulphate
  9. filtrationfiltered through silica gel

출처 및 근거

ORD 기록
ord-34d51ce229a14615baf7b0af6c984163
출처 데이터셋
uspto-grants-1980_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04213993

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