반응 #4556

ord-53fcb22988bf4f00ace4b323695f617b

반응 방정식

Oc1ccccc1
phenol
Cl
HCl
[Br-]
bromide
O=C([O-])[O-]
carbonate
Oc1ccc(Oc2ccc(Cl)cc2F)cc1
4-(4-chloro-2-fluorophenoxy)phenol
CCOC(=O)CCC(C)Br
ethyl 4-bromopentanoate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
CCOC(=O)CCC(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
ester
CCOC(=O)CCC(C)Oc1ccc(Oc2ccc(Cl)cc2F)cc1
Ethyl 4-(4-(4-Chloro-2-fluorophenoxy)phenoxy)pentanoate

용매

반응 조건

온도
130°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타had reacted
  2. 2
    온도After cooling
  3. 3
    추출the product extracted into a 1:1 mixture of ether-pentane (2×150 ml)
  4. 4
    세척washed with 10% NaOH solution (200 ml)
  5. 5
    건조dried (MgSO4)
  6. 6
    기타the solvent evaporated
  7. 7
    기타The resulting orange oil was purified via preparative HPLC (9:1 hexane/ethyl acetate) with the second peak
  8. 8
    기타being collected
  9. 9
    기타Removal of the solvent

실험 절차

A stirred mixture of 4-(4-chloro-2-fluorophenoxy)phenol (2.3 g, 0.0103 mol), ethyl 4-bromopentanoate (2.01 g, 0.0103 mol), and potassium carbonate (1.46 g, 0.105 mol) in DMF (20 ml) was heated in an oil bath at 130° C. for one hour. Additional bromide (0.5 g) and carbonate (0.5 g) were added each hour for the next four hours. At the end of this period, gas chromatography indicated that most of the starting phenol had reacted. After cooling, the reaction mixture was poured into 4N HCl solution (200 ml), and the product extracted into a 1:1 mixture of ether-pentane (2×150 ml). The organic extracts were combined, washed with 10% NaOH solution (200 ml), dried (MgSO4), then the solvent evaporated. The resulting orange oil was purified via preparative HPLC (9:1 hexane/ethyl acetate) with the second peak being collected. Removal of the solvent gave the desired ester as a light yellow oil: RI=1.5344 @ 25° C. Calc: C, 62.21; H, 5.50. Found: C, 62.38; H, 5.33.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04725683uspto-grants-1988_02