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HRID 2856Erstellt: 23. Oktober 2026
Vinyl chloroformate → (+/-)-trans-4a-(3-Methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochloride
https://huagongshe.com/de/reaction/2856
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Vinyl chloroformate | HCID 78808 | — |
| Edukt | Proton sponge | HCID 88675 | — |
| Edukt | (+/-)-trans-1,2,3,4,4a,5,6,7,8,8a-Decahydro-2-ethyl-4a-(3-methoxyphenyl)-6-isoquinolinone | HCID 10517409 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | (+/-)-trans-4a-(3-Methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8, 8a-decahydroisoquinoline hydrochloride | HCID 86752321 | 70,8% |
Reaktionsschritte
A solution of 1.2 g (4.2 mmol) of (±)-trans-2-ethyl-4a-(3-methoxyphenyl)-6-oxo-1,2,3,4,4a,5,6,7,8,8a-decahydroisoquinoline and 1.8 g (12.6 mmol) of proton sponge in 34 ml of 1,2-dichloroethane was treated with 1.4 ml (16.8 mmol) of vinylchloroformate at 0° C. under nitrogen atmosphere. The reaction mixture was stirred at this temperature for 15 min and then refluxed for 3 h, the solvent was removed in vacuo, the residue was taken up in water and extracted with Et2O. The organic layer was washed with 3% HCl, then was dried over Na2SO4 and the solvent was removed in vacuo. The dark residue was dissolved in EtOH, 3 ml of concentrated HCl were added and the solution refluxed for 3 hours. The solvent was removed in vacuo, obtaining 0.88 g of the title compound which was used as such in the subsequent step. M.p.=90° C. dec.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05731322 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-65c40f72159b46c38bd188c224445f20 |
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| Quellennotiz | uspto-grants-1998_03 |
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