تفاعل #4001
ord-cb342278cc67421d861b38254858d7ca
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةheated under nitrogen
- 2أخرىpurge as the bath temperature
- 3أخرىapproached 100° C.
- 4أخرىreaction
- 5أخرىWhen the initial reaction
- 6workup.WAITsubsided after a few minutes
- 7درجة الحرارةthe bath temperature was raised to 130° C.
- 8أخرىas indicated by cessation of gassing (about 1 hour)
- 9درجة الحرارةto cool about 60° C.
- 10استخلاصThe solution was extracted with 500 parts of ethyl acetate
- 11workup.ADDITIONThe aqueous phase was treated with decolourising charcoal
- 12ترشيحfiltered
- 13workup.ADDITIONthe pH was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate solution
- 14ترشيحThe precipitated solid was filtered
- 15غسيلwashed with water
- 16أخرىdried to constant weight at 80° C. in a vacuum oven
الإجراء التجريبي
620 parts of 4-chloro-4-chloromethyloxetan-2-one and 440 parts of guanidine hydrochloride were charged to a reaction flask and the mixture was stirred and heated under nitrogen purge as the bath temperature was gradually raised to 120° C. When the bath temperature approached 100° C., reaction commenced accompanied by evolution of hydrogen chloride. When the initial reaction subsided after a few minutes the bath temperature was raised to 130° C. and held until the reaction ceased as indicated by cessation of gassing (about 1 hour). The reaction mixture was allowed to cool about 60° C. and 1750 parts of water was added to the syrup. The solution was extracted with 500 parts of ethyl acetate and the extract was discarded. The aqueous phase was treated with decolourising charcoal, filtered and the pH was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate solution. The precipitated solid was filtered, washed with water and dried to constant weight at 80° C. in a vacuum oven to give 2-amino-4-chloromethyl-6-hydroxypyrimidine, m.p. 195°-197° C.