HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5859Generated: October 26, 2026
Phosgene → 4-(1-Naphthyl)-1-[3-(1,2,3,4-tetrahydro-5-naphthylcarbamoyloxy)propyl]piperazine, hydrochloride
https://huagongshe.com/reaction/5859
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 5-Tetralinylamine | HCID 16671 | — |
| Reactant | 4-(1-Naphthalenyl)-1-piperazinepropanol | HCID 12217536 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(1-Naphthyl)-1-[3-(1,2,3,4-tetrahydro-5-naphthylcarbamoyloxy)propyl]piperazine, hydrochloride | HCID 131718167 | — |
Reaction Steps
A mixture of 5-amino-1,2,3,4-tetrahydronaphthalene (300 mg; 2.0 mmol) in toluene (10 ml) and phosgene (10 ml 20% in toluene) was refluxed for 6 h. The solvent was removed under reduced pressure to give crude 1,2,3,4-tetrahydronaphthyl -5-isocyanate. To the crude product was added 3-[4-(1-naphthyl)-1-piperazinyl]propanol (240 mg; 2.0 mmol) in toluene (60 ml) and refluxed for 6 h. The reaction mixture was then concentrated and submitted to flash chromatography on silica gel 60 eluting with dichloromethane graduated to dichloromethane/ethyl acetate (1:1). The product was taken up in ethanol, which was treated with hydrogen chloride in ether to give 340 mg of the title compound. M.p. 227°-229° C. MS (70 eV): m/z 443 (M+,46), 270 (39), 225 (100), 173 (45), 145 (31), 127 (21), 114 (31), 70 (80).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05246935 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-a2ccd79bcb014e29be695973b6182ff8 |
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| Source note | uspto-grants-1993_09 |
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