تفاعل #1647

ord-32e98db4036848ce8b8264c0ec0c3131

معادلة التفاعل

CCOC(C)=O
ethyl acetate
Cc1cn(COCOC(=O)c2ccccc2)c(=O)[nH]c1=O
1-[(benzoyloxy)methoxymethyl]thymine
CCC(CC)OP(=O)(O)O
diethyl phosphonomethanol
C[Si](C)(C)OS(=O)(=O)C(F)(F)F
trimethylsilyl trifluoromethanesulfonate
CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
title compound
CCOP(=O)(COCOCn1cc(C)c(=O)[nH]c1=O)OCC
1-[(Diethylphosphonomethoxy)methoxymethyl]thymine

المذيبات

ظروف التفاعل

درجة الحرارة
85°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooling to room temperature
  2. 2
    غسيلwashed with aqueous bicarbonate, brine
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    ترشيحfiltered
  5. 5
    تركيزconcentrated in vacuo
  6. 6
    أخرىThe resultant yellow oil was purified by silica gel column chromatography

الإجراء التجريبي

To a solution of 1-[(benzoyloxy)methoxymethyl]thymine (2.9 g, 10 mmol) and diethyl phosphonomethanol (1.85 g, 11 mmol) in benzene (180 mL) was added trimethylsilyl trifluoromethanesulfonate (0.05 mL) via a syringe under nitrogen. The solution was heated at 85° C. for 20 min. After cooling to room temperature, ethyl acetate (50 mL) was added and washed with aqueous bicarbonate, brine dried (MgSO4), filtered and concentrated in vacuo. The resultant yellow oil was purified by silica gel column chromatography using CH2Cl2 /5% MeOH as an eluent to give the title compound as a white oil: yield 980 mg (30%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05726174uspto-grants-1998_03