HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357321Generated: October 25, 2026
Isopropanol → 4-(Piperazinylmethyl)styrene
https://huagongshe.com/reaction/357321
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Benzene, 1-(chloromethyl)-3(or 4)-ethenyl- | HCID 11768772 | — |
| Product | 4-(Piperazinylmethyl)styrene | HCID 3332880 | — |
Reaction Steps
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 10.135 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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840766 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-262f09c9021d43c681517d4600bdd730 |
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| Source note | uspto-grants-1998_11 |
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