Реакция #51860

Уравнение реакции

Water

triethylamine

(2-chlorosulfonyl-4,5-dimethoxy-phenyl)-acetic acid benzyl ester

morpholine

→

title compound

Выход 60.2%

[4,5-Dimethoxy-2-(morpholine-4-sulfonyl)-phenyl]-acetic acid benzyl ester

Выход 60.2%

Растворители

tetrahydrofuran

tetrahydrofuran

Условия реакции

Обработка

1. 1
   Другоеto form a solid mass
2. 2
   workup.ADDITIONwas added
3. 3
   Температураthe mixture was warmed to ambient temperature over 20 hours
4. 4
   Экстракцияextracted with ethyl acetate (2×100 cm3)
5. 5
   СушкаThe combined ethyl acetate extracts were dried over sodium sulfate, vacuum
6. 6
   Фильтрацияfiltered
7. 7
   Другоеthe filtrate volatile fractions removed in vacuo
8. 8
   Другоеto afford a crude tan solid
9. 9
   ДругоеThe crude solid was recrystallized from toluene (150 cm3)

Методика

To a stirred mixture of (2-chlorosulfonyl-4,5-dimethoxy-phenyl)-acetic acid benzyl ester (15.0 g, 39.0 mmol) in anhydrous tetrahydrofuran (45 cm3) cooled to 0° C. in an ice bath under an atmosphere of dry nitrogen was added triethylamine (6.00 cm3, 43 mmol). The mixture was stirred 2 minutes and morpholine (3.75 cm3, 43 mmol) was added dropwise to form a solid mass. To efficiently stir the mixture additional anhydrous tetrahydrofuran (145 cm3) was added and the mixture was warmed to ambient temperature over 20 hours. Water was added to the mixture and extracted with ethyl acetate (2×100 cm3). The combined ethyl acetate extracts were dried over sodium sulfate, vacuum filtered and the filtrate volatile fractions removed in vacuo to afford a crude tan solid. The crude solid was recrystallized from toluene (150 cm3) to afford the title compound as tan crystals (10.2 g, 60.2%) with a positive ion ESI (M+H)+436.2.

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