반응 #72447

ord-bf9317006e5b4b4a9b4ea276933792a1

반응 방정식

Oc1ccc(-c2cc(=S)ss2)cc1
4-hydroxyphenylisothiocyanate
Oc1ccc(-c2cc(=S)ss2)cc1
5-p-hydroxyphenyl-1,2-dithiole-3-thione
COc1ccc2cc([C@H](C)C(=O)O)ccc2c1
naproxene
Oc1cccc2[nH]nnc12
hydroxybenzotriazole
C(=NC1CCCCC1)=NC1CCCCC1
DCC
COc1ccc2cc(C(C)C(=O)Oc3ccc(N=C=S)cc3)ccc2c1
4-(isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate

반응 조건

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

후처리

  1. 1
    workup.STIRRINGstirred for 1 h at 0° C. and 2 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
    기타the precipitate was removed
  7. 7
    기타The solvent was evaporated
  8. 8
    세척eluted with dichloromethane, from which 4-(isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate (3)
  9. 9
    기타was obtained
  10. 10
    기타(230 mg, 21 yield)

실험 절차

To the solution of 1 (naproxene, 691 mg, 3 mmol) in 20 mL of dimethylformamide, hydroxybenzotriazole (446 mg, 3.3 mmol) and DCC (619 mg, 3.3 mmol) were added with stirring at 0° C. for 1 h. To the reaction mixture 4-hydroxyphenylisothiocyanate (2; 500 mg, 3.3 mmol) was added and stirred for 1 h at 0° C. and 2 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 ethyl acetate and the precipitate was removed. The solvent was evaporated and the crude product was loaded on a silica gel open column and eluted with dichloromethane, from which 4-(isothiocyano)-phenyl 2-(2-methoxynaphthalen-6-yl)propanoate (3) was obtained (230 mg, 21 yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08541398B2uspto-grants-2013_09