تفاعل #5341

ord-3ef2cd7b916a450b941ab84417ba43f7

معادلة التفاعل

O=C1COC(=O)C1
tetronic acid
CCN(CC)CC
triethylamine
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CCCCCCOc1ccc(OCCCCCC(=O)O)cc1
6-[4-(hexyloxy)phenoxy]hexanoic acid
Cl
HCl
O=C(CCCCCOc1ccc(Cl)cc1)C1=C(O)COC1=O
4-hydroxy-3-[6-(4-chlorophenoxy)-1-oxohexyl]-2(5H)-furanone
المردود 43.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصextracted three times with ether
  2. 2
    تجفيفThe combined organic layers are dried over MgSO4
  3. 3
    تركيزconcentrated in vacuo
  4. 4
    أخرىgiving a yellow solid
  5. 5
    ترشيحfiltering

الإجراء التجريبي

To a stirring solution of 554 mg (5.54 mmol) of tetronic acid in 20 mL of diemthylformamide is added 850 μL (6.09 mmol) of triethylamine and 220 mg (1.765 mmol) of 4-dimethylaminopyridine at 0° C. Next, 1.26 g (6.63 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride and 1.475 g (6.63 mmol) of 6-[4-(hexyloxy)phenoxy]hexanoic acid are added and the reaction mixture is stirred 2 days at room temperature. The reaction is acidified with 1.0N HCl and extracted three times with ether. The combined organic layers are dried over MgSO4 and concentrated in vacuo giving a yellow solid. Pure material is obtained by trituration in ether, filtering to give 774 mg (43%) of 4-hydroxy-3-[6-(4-chlorophenoxy)-1-oxohexyl]-2(5H)-furanone.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05242945uspto-grants-1993_09