HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 2-Bromomethyl-6-methoxybenzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 2-Amino-5-methoxybenzene-1-thiol | HCID 235509 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromomethyl-6-methoxybenzothiazole | HCID 10706323 | — |
Reaction Steps
7.75 g (50 mmol) of 2-amino-5-methoxy-thiophenol are dissolved in 150 ml methylene chloride and 14.1 g (70 mmol) of bromoacetylbromide are added whilst cooling with ice. Then the mixture is heated for 1 hour to reflux temperature. After cooling solid potassium carbonate is added until foaming ceases, the mixture is filtered and the filtrate is evaporated down. The evaporation residue is purified by column chromatography on neutral aluminium oxide (eluant: petroleum ether/ethyl acetate=3:1). Yield: 6.8 g (52.7 of theory), Melting point: 90-91° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919807 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-c4912c173d144ac6b3e261b9afa35f1c |
| Source note | uspto-grants-1999_07 |