HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973551Generated: November 2, 2026
2-((1-Naphthalenyloxy)methyl)oxirane → HCID 11596312, compound
https://huagongshe.com/reaction/1973551
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-((1-Naphthalenyloxy)methyl)oxirane | HCID 91521 | — |
| Reactant | 1-(4-Methoxyphenyl)piperazine | HCID 269722 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11596312 | HCID 11596312 | 76% |
Reaction Steps
20.0 g. (0.1 mol) 2,3-epoxy-1-(1-naphthyloxy)-propane were mixed with 30 ml. ethanol and 19.2 g. (0.1 mol) 1-(4-methoxyphenyl)-piperazine, whereafter the reaction mixture was heated to 60° C. and maintained at this temperature for 6 hours. The reaction mixture was then left to stand overnight and the ethanol subsequently evaporated off. The oily residue was dissolved in chloroform, hydrogen chloride was passed through the chloroform solution and then ether was added, the dihydrochloride thereby precipitating out. This was filtered off with suction and recrystallized from methanol/ethanol (1:3). There was obtained 1-(4-methoxy-phenyl)-4-[3-(naphth-1-yloxy)-2-hydroxypropyl]-piperazine in a yield of 76% of theory. The product had a melting point of 237° - 238° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03997666 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-b3ca571efe2647fbb000104fe8b64fe9 |
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| Source note | uspto-grants-1976_12 |
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