تفاعل #1104
ord-77b579259b0e47c2ac2dc691717deb93
معادلة التفاعل
HCl
4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine
THF
magnesium
4-tert-butylbenzyl bromide
→
4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1استخلاصthe mixture is extracted several times with ethyl acetate
- 2غسيلthe combined ethyl acetate phases are washed with sodium hydrogen carbonate solution
- 3أخرىPurification
- 4درجة الحرارةincreasing amounts of methanol
- 5workup.ADDITIONare added
الإجراء التجريبي
A Grignard solution is prepared from 1.2 g of magnesium and 12.9 g of 90% strength 4-tert-butylbenzyl bromide in 100 ml of abs. ether. 2.9 g of 4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine in 50 ml of absolute THF are added dropwise to this solution. After 17 hours at room temperature it is acidified with 25 ml of 2N HCl, the mixture is extracted several times with ethyl acetate and the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution. Purification is carried out by column chromatography on silica gel using ethyl acetate to which increasing amounts of methanol are added.