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Nitric Acid → 3-Chloro-6-nitrotoluene

HRID 1773573
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HRID 1773573 반응식
[N+:1]([O-:4])([OH:3])=[O:2].[Cl:5][C:6]1[CH:7]=[C:8]([CH3:12])[CH:9]=[CH:10][CH:11]=1.S(=O)(=O)(O)O>C(O)(=O)C>[Cl:5][C:6]1[CH:7]=[C:8]([CH3:12])[CH:9]=[CH:10][C:11]=1[N+:1]([O-:4])=[O:2].[Cl:5][C:6]1[CH:11]=[CH:10][C:9]([N+:1]([O-:3])=[O:2])=[C:8]([CH3:12])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 944Nitric AcidHCID 1118Sulfuric AcidHCID 79313-Chlorotoluene

생성물 2

HCID 793293-Chloro-6-nitrotoluene수율 39%HCID 1234783-Chloro-4-nitrotoluene수율 14%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Concentrated nitric acid (16 mL) was slowly added, at 0° C., to a solution of 3-chlorotoluene (3 mL, 25.4 mmol) and concentrated sulfuric acid (6 mL) in glacial acetic acid (20 mL) and the resulting mixture was stirred for 24 hours allowing the temperature to rise until room temperature. The reaction mixture was then poured into ice-water and partitioned between water and diethyl ether. The aqueous phase was separated and extracted twice with diethyl ether; the combined organic extracts were washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The yellow oily residue was purified on a silica gel plug and twice by flash chromatography to give 1.22 g (14% yield) of 2-chloro-4-methyl-1-nitro-benzene as a yellow oil and 3.39 g (39% yield) of 4-chloro-2-methyl-1-nitro-benzene.

후처리

  1. customto rise until room temperature
  2. custompartitioned between water and diethyl ether
  3. customThe aqueous phase was separated
  4. extractionextracted twice with diethyl ether
  5. washthe combined organic extracts were washed with water and brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customevaporated under reduced pressure
  9. customThe yellow oily residue was purified on a silica gel plug and twice by flash chromatography

출처 및 근거

ORD 기록
ord-dc4775633c1d4cd497d84368ba7831d2
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09255110B2

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