HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 2-(2,1,3-Benzoxadiazol-5-yloxy)nicotinic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | 2-(Benzo[2,1,3]oxadiazol-5-yloxy)-nicotinic acid ethyl ester | HCID 23529345 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2,1,3-Benzoxadiazol-5-yloxy)nicotinic acid | HCID 22610138 | 95.8% |
Reaction Steps
A solution of 2-(benzo[2,1,3]oxadiazol-5-yloxy)-nicotinic acid ethyl ester (2.2 g) in tetrahydrofuran (75 mL) was treated with 1M aqueous lithium hydroxide (23.1 mL) at ambient temperature for 16 h. The solution was concentrated in vacuo to remove the tetrahydrofuran, and then acidified with 1N hydrochloric acid. The resulting precipitate was filtered and dried to give the title compound (1.90 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07250518B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-56eb0954c9464447ad4884db67a91c1c |
| Source note | uspto-grants-2007_07 |