HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 1-Naphthol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Duloxetine | HCID 60835 | — |
| Product | 1-Naphthol | HCID 7005 | — |
| Product | Thiophen-2-ol | HCID 10909502 | — |
Reaction Steps
Duloxetine is acid labile, and acid hydrolysis of its ether linkage results in a thienyl alcohol and 1-naphthol. 50% of a dosage is hydrolyzed to 1-naphthol within one hour at a pH of 1.0, which is achieved under fasting conditions. At a pH of 2.0, 10% of the dosage degrades to 1-Naphthol in one hour and at a pH of 4.0, 10% degradation would take up to 63 hours. The reaction scheme showing the conversion of duloxetine to 1-naphthol and its thienyl derivative is shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08455667B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-d99e2984a6364751b8b8ccf7f34786e0 |
| Source note | uspto-grants-2013_06 |