Реакция #51859

Уравнение реакции

triethylamine

benzyl alcohol

3,4-dimethoxyphenylacetic acid

thionyl chloride

→

title compound

Выход 60.1%

(3,4-Dimethoxy-phenyl)-acetic acid benzyl ester

Выход 60.1%

Растворители

Water

dichloromethane

dichloromethane

1,2-dichloroethane

Условия реакции

Обработка

1. 1
   ТемператураThe resulting solution was heated
2. 2
   Температураto reflux for 16 hours
3. 3
   Другоеthe volatile fractions removed in vacuo
4. 4
   ДругоеResidual thionyl chloride was removed by an azeotrope with toluene (3×200 cm3)
5. 5
   Другоеto afford a crude brown oil
6. 6
   Температураcooled to 0° C. in an ice bath
7. 7
   Температураwarmed to ambient temperature
8. 8
   Экстракцияthe aqueous extracted with dichloromethane (2×100 cm3)
9. 9
   СушкаThe combined dichloromethane extracts were dried over sodium sulfate, vacuum
10. 10
    Фильтрацияfiltered
11. 11
    Другоеthe filtrate volatile fractions removed in vacuo
12. 12
    Другоеto afford a crude brown oil
13. 13
    ДругоеThe crude product was purified by column chromatography (silica, eluting with hexane-ethyl acetate 1:0 to 1:1)

Методика

To a stirred mixture of commercially available 3,4-dimethoxyphenylacetic acid (100.0 g, 510 mmol) in anhydrous 1,2-dichloroethane (500 cm3) at ambient temperature under an atmosphere of dry nitrogen was added thionyl chloride (112 cm3, 1.53 mol) portionwise over 20 minutes. The resulting solution was heated to reflux for 16 hours. The brown solution was cooled to ambient temperature and the volatile fractions removed in vacuo. Residual thionyl chloride was removed by an azeotrope with toluene (3×200 cm3) to afford a crude brown oil. The crude oil was dissolved in anhydrous dichloromethane (400 cm3) and cooled to 0° C. in an ice bath. To the cooled solution was added triethylamine (75 cm3, 535 mmol) dropwise over 10 minutes followed by a solution of benzyl alcohol (50 cm3, 485 mmol) dissolved in anhydrous dichloromethane (200 cm3). The mixture was stirred for 20 hours and warmed to ambient temperature. Water was added to the mixture (700 cm3) and the aqueous extracted with dichloromethane (2×100 cm3). The combined dichloromethane extracts were dried over sodium sulfate, vacuum filtered and the filtrate volatile fractions removed in vacuo to afford a crude brown oil. The crude product was purified by column chromatography (silica, eluting with hexane-ethyl acetate 1:0 to 1:1) to afford the title compound as a pale yellow viscous oil (83.4 g, 57.2%) with a positive ion ESI (M−1H)+287.3.

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