반응 #46907

ord-11293029832f43868d0ac3067b1a6d6f

반응 방정식

NC(=O)c1ccc(O)cc1
4-hydroxybenzamide
CC(=O)Oc1ccccc1C(=O)O
acetylsalicylic acid
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
C(=NC1CCCCC1)=NC1CCCCC1
DCC
CC(=O)Oc1ccccc1C(=O)Oc1ccc(C(N)=O)cc1
4-carbamoylphenyl 2-acetoxybenzoate
수율 47.0%

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGstirred for 1 h at 0° C. and 3 h at room temperature
  2. 2
    여과After filtration
  3. 3
    기타the filtrate was evaporated under reduced pressure
  4. 4
    기타to remove the solvent
  5. 5
    기타The oily residue thus obtained
  6. 6
    세척the organic layer was washed with brine
  7. 7
    건조dried on anhydrous MgSO4
  8. 8
    여과filtered
  9. 9
    기타the solvent evaporated
  10. 10
    세척eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-acetoxybenzoate (5)
  11. 11
    기타was obtained (410 mg, 47% yield)

실험 절차

To the solution of 1 (acetylsalicylic acid, 500 mg, 2.77 mmol) in 15 mL of dimethylformamide, hydroxybenzotriazole (412 mg, 3.05 mmol) and DCC (628 mg, 3.05 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxybenzamide (4, 418 mg, 3.05 mmol) was added and stirred for 1 h at 0° C. and 3 h at room temperature. After filtration, the filtrate was evaporated under reduced pressure to remove the solvent. The oily residue thus obtained was dissolved in chloroform; the organic layer was washed with brine, dried on anhydrous MgSO4, filtered and the solvent evaporated. The crude product 5 was loaded on a silica gel open column and eluted with CH2Cl2/MeOH (9/1), from which 4-carbamoylphenyl 2-acetoxybenzoate (5) was obtained (410 mg, 47% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07741359B2uspto-grants-2010_06