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Hydrochloric Acid → 4-(2-Oxopropyl)benzoic acid

HRID 1906956
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HRID 1906956 반응식
Cl.[C:2]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]=[C:12]([N+]([O-])=O)[CH3:13])=[CH:7][CH:6]=1)([OH:4])=[O:3].[OH2:17]>O1CCOCC1.[Fe]>[CH2:11]([C:8]1[CH:9]=[CH:10][C:5]([C:2]([OH:4])=[O:3])=[CH:6][CH:7]=1)[C:12]([CH3:13])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 542582771-(4-Carboxyphenyl)-2-nitropropene

생성물 1

HCID 5762444-(2-Oxopropyl)benzoic acid

시약·촉매·용매 2

HCID 23925Iron촉매HCID 312751,4-Dioxane용매

실험 절차

Concentrated hydrochloric acid (367 ml) was added dropwise to a mixture of 1-(4-carboxyphenyl)-2-nitroprop-1-ene (61.17 g) and iron powder (61.17 g) in dioxan (500 ml) at reflux. The heating was continued for 1 hour at the end of addition. The solution was cooled, water added, the dioxan evaporated and the residue extracted with chloroform and dried (MgSO4). Removal of the solvent gave a solid which was recrystallised from ethyl acetate to give 26 g of the title compound. τ(d6DMSO) 7.83 (3H, s), 6.14 (2H, s), 2.69 (2H, d, J=9 Hz), 2.05 (2H, d, J=9 Hz).

후처리

  1. temperatureat reflux
  2. additionThe heating was continued for 1 hour at the end of addition
  3. temperatureThe solution was cooled
  4. customthe dioxan evaporated
  5. extractionthe residue extracted with chloroform
  6. dry with materialdried (MgSO4)
  7. customRemoval of the solvent
  8. customgave a solid which
  9. customwas recrystallised from ethyl acetate

출처 및 근거

ORD 기록
ord-3698451d0b59465b847a4f970c594426
출처 데이터셋
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04654371

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