HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Morphine 6-glucuronide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Morphine | HCID 5288826 | — |
| Reactant | aldehydo-D-glucuronate | HCID 5460126 | — |
| Reactant | Azane;hydrate | HCID 12896473 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | n-BuOH acetone AcOH | HCID 86750706 | — |
| Product | Morphine 6-glucuronide | HCID 5360621 | 52% |
Reaction Steps
To a solution of the above glucuronate in MeOH (24 ml) was added 5% aqueous NaOH (6 ml) and the mixture was left to stir for 20 hours. T.l.c (n-BuOH/acetone/AcOH/5% aq.NH3 /water 45:15:10:10:20) showed that there were two components one of which was M6G and the other morphine. The solution was transferred to a beaker and was acidified with glacial acetic acid (7 ml) which took the pH of the mixture to 5.5. Shortly after this pH was reached (5 minutes), a white solid started to precipitate. The suspension was stirred for a further 30 minutes, the solid filtered and washed with MeOH, and morphine-6-glucuronide (0.4 g, 52%) was obtained after drying at 120° C. for 4 hours, m.p. 240°-243° C. More M6G could be obtained by cooling the filtrate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05621087 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-5a44e8790619407d8231ff3ebcf9fef6 |
| Source note | uspto-grants-1997_04 |