تفاعل #1669592

ord-893932b2e0e04472ae811988e4540847

معادلة التفاعل

CCOC(=O)c1sc(C(=O)OCC)c(O)c1O
3,4-dihydroxythiophene-2,5-dicarboxylic acid diethyl ester
OCCO
ethylene glycol
CCOC(=O)c1sc(C(=O)OCC)c2c1OCCO2
2,3-dihydro-thieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid diethyl ester
المردود 95.3%

المذيبات

ظروف التفاعل

درجة الحرارة
25°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةrefluxed for 9 h
  2. 2
    تركيزconcentrated by rotary evaporator
  3. 3
    أخرىto remove the THF
  4. 4
    workup.ADDITIONThe residue was diluted with diethyl ether
  5. 5
    workup.WAITto stand overnight
  6. 6
    أخرىto precipitate out
  7. 7
    أخرىThe tributylphosphine oxide was then removed by filtration
  8. 8
    أخرىthe residue purified by chromatography on silica gel (eluant: ethyl acetate/ hexane=2/1)

الإجراء التجريبي

ADC01 (2.9 g, 16.9 mmol) was slowly added to a solution of 3,4-dihydroxythiophene-2,5-dicarboxylic acid diethyl ester (2.0 g, 7.7 mmol), ethylene glycol (0.5 g, 8.5 mmol), and PHOL (3.4 g, 16.9 mmol) in dry tetrahydrofuran (150 ml) at 25° C. The reaction mixture was stirred for 3 h and then refluxed for 9 h. The reaction mixture was allowed to cool to 25° C. and concentrated by rotary evaporator to remove the THF. The residue was diluted with diethyl ether and allowed to stand overnight to enable the tributylphosphine oxide to precipitate out. The tributylphosphine oxide was then removed by filtration and the residue purified by chromatography on silica gel (eluant: ethyl acetate/ hexane=2/1) to give 2.1 g of 2,3-dihydro-thieno[3,4-b][1,4]dioxine-5,7-dicarboxylic acid diethyl ester as white crystals (95% yield) as fully characterized by 1H NMR, 13C NMR, HRMS, and elemental analysis.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06734312B2uspto-grants-2004_05