تفاعل #51860

معادلة التفاعل

Water

triethylamine

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

morpholine

→

title compound

المردود 60.2%

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

المردود 60.2%

المذيبات

tetrahydrofuran

tetrahydrofuran

ظروف التفاعل

المعالجة

1. 1
   أخرىto form a solid mass
2. 2
   workup.ADDITIONwas added
3. 3
   درجة الحرارةthe mixture was warmed to ambient temperature over 20 hours
4. 4
   استخلاصextracted with ethyl acetate (2×100 cm3)
5. 5
   تجفيفThe combined ethyl acetate extracts were dried over sodium sulfate, vacuum
6. 6
   ترشيحfiltered
7. 7
   أخرىthe filtrate volatile fractions removed in vacuo
8. 8
   أخرىto afford a crude tan solid
9. 9
   أخرىThe crude solid was recrystallized from toluene (150 cm3)

الإجراء التجريبي

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.

المصدر