HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hydroxide → 3,4-Dimethylbenzothiazol-2-one-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 3,4-dimethylbenzothiazol-2-one-5-carboxylate | HCID 22390078 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-Dimethylbenzothiazol-2-one-5-carboxylic acid | HCID 22390083 | 83.7% |
Reaction Steps
A solution of 10.15 g (43 mmol) of methyl 3,4-dimethylbenzo-thiazol-2-one-5-carboxylate in 100 ml of tetrahydrofuran and 100 ml of water was admixed with 2.06 g (86 mmol) of lithium hydroxide. The solution was then heated at reflux for 2 hours. After cooling, the tetrahydrofuran was removed under reduced pressure, the remaining aqueous solution was acidified and the precipitated solid was filtered off with suction and dried. More product was obtained by extracting the mother liquor with ethyl acetate. This gave a total of 8 g (36 mmol, 83% yield) of 3,4-dimethylbenzothiazol-2-one-5-carboxylic acid of m.p. 235° C.-239° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908884B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-0e5a17ca05fa4c5a8b3ee901968bfa26 |
| Source note | uspto-grants-2005_06 |