반응 #5346

ord-fe7b1958be8d4b2ab72860d32d3007d3

반응 방정식

O=C1COC(=O)C1
tetronic acid
CCN(CC)CC
triethylamine
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
O=C(O)CCCCCCCCOc1ccc(Cl)cc1
9-(4-chlorophenoxy)nonanoic acid
Cl
HCl
O=C(CCCCCCCCOc1ccc(Cl)cc1)C1=C(O)COC1=O
3-[9-(4-chlorophenoxy)-1-oxononyl]4-hydroxy-2(5H)-furanone
수율 30.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출extracted with four 50 mL portions of ether
  2. 2
    건조The combined organic layers are dried over MgSO4
  3. 3
    농축concentrated in vacuo
  4. 4
    기타affording crude compound

실험 절차

To a stirring solution of 736 mg (7.36 mmol) of tetronic acid in 30 mL of dimethylformamide is added 1.2 mL (8.09 mmol) of triethylamine and 300 mg of 4-dimethylaminopyridine at 0° C. Next, 1.7 g (8.86 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 2.6 g (8.06 mmol) of 9-(4-chlorophenoxy)nonanoic acid are added and the reaction is stirred overnight at room temperature. The reaction is acidified with 1.0 N HCl and extracted with four 50 mL portions of ether. The combined organic layers are dried over MgSO4 and concentrated in vacuo affording crude compound. Pure material is obtained by flash chromatography with 10% methanol/ethyl acetate as eluant affording 800 mg (30%) of 3-[9-(4-chlorophenoxy)-1-oxononyl]4-hydroxy-2(5H)-furanone.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05242945uspto-grants-1993_09