Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21474319 | HCID 21474319 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21474457 | HCID 21474457 | — |
Reaction Steps
1.9 ml of 37% conc. HCl are poured over 0.19 g of 3-benzyloxy-1-(2-hydroxy-ethyl)-2-[hydroxy-(4-nitro-phenyl)-methyl]-1H-pyridin-4-one. The mixture is heated with stirring at 100° C. for 45 minutes. 20 ml of toluene are added and distillation is carried out at a bath temperature of 50° C. and under a pressure of 60 mbar using a rotary evaporator. The addition of toluene and the distillation are repeated four times. The crystalline residue is recrystallised from ethanol, yielding 3-hydroxy-1-(2-hydroxy-ethyl)-2-[hydroxy-(4-nitro-phenyl)-methyl]-1H-pyridin-4-one hydrochloride. Brown crystals, m.p.: from 204° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688815 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-d10d7ff4e532490da3ccd6fda3ef6e59 |
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| Source note | uspto-grants-1997_11 |
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