反応 #83670

反応方程式

vinylbenzyl chloride

piperazine

isopropanol

→

4-(piperazinylmethyl)styrene

反応条件

後処理

1. 1
   温度cooled slowly to room temperature
2. 2
   その他to form a slurry of crystalline material
3. 3
   ろ過filtered
4. 4
   その他dried
5. 5
   濃縮The mother liquor was concentrated to about 25 mL on a rotary evaporator and ethyl acetate (50 mL)
6. 6
   workup.ADDITIONwas added)
7. 7
   workup.WAITThe resulting mixture was refrigerated for about 10 minutes
8. 8
   ろ過after which a second crop of piperazine hydrochloride was filtered off
9. 9
   その他The mother liquor was then evaporated to dryness on a rotary evaporator

実験手順

To a 500 mL flask was added vinylbenzyl chloride (7.63 g, 0.050 mol), piperazine (8.61 g, 0.100 mol), and isopropanol (50 mL). The resulting solution was heated to 70° C. for 45 minutes and then cooled slowly to room temperature to form a slurry of crystalline material. The slurry was refrigerated for about three hours and then filtered. The solid piperazine hydrochloride salt was vacuum dried and then weighed (5.55 g) and discarded. The mother liquor was concentrated to about 25 mL on a rotary evaporator and ethyl acetate (50 mL) was added). The resulting mixture was refrigerated for about 10 minutes, after which a second crop of piperazine hydrochloride was filtered off and discarded. The mother liquor was then evaporated to dryness on a rotary evaporator to afford 10.35 g of crude 4-(piperazinylmethyl)styrene which was used without further purification to prepare N-(4-methylstyrene)-N'-(3-trimethylammonio-2-hydroxypropyl chloride)piperazine as follows.

出典