HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-(5-Chloropentyloxy)benzo[d]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-5-chloropentane | HCID 96070 | — |
| Reactant | HCID 178517143 | HCID 178517143 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(5-Chloropentyloxy)benzo[d]thiazole | HCID 71529585 | — |
Reaction Steps
To a solution of 2-hydroxybenzothiazole (0.2 g, 1.32 mmol) in 10 mL of acetonitrile was added K2CO3 (0.274 g, 1.98 mmol), followed by stirring at 50˜55° C. for 30 min. Then, 1-bromo-5-chloropentane (0.245 g, 1.32 mmol) was added to and reacted with the solution of 2-hydroxybenzothiazole at 80˜90° C. for 3 hours. The reaction was cooled to room temperature, diluted with 10 mL of EtOAc, and washed with distilled water and a saturated NaCl aqueous solution. It was dried over MgSO4 and the solvent was removed by concentration under reduced pressure to afford K23 (0.333 g, 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604214B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-5c9542e12e5648b8b7309b1726867a5b |
| Source note | uspto-grants-2013_12 |