HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-(Chloromethyl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Methyl 2-chloroethanimidate--hydrogen chloride (1/1) | HCID 12680765 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Chloromethyl)benzothiazole | HCID 304978 | 71.1% |
Reaction Steps
To a solution of aminothiophenol (8.3 g) in methylene chloride at 0° C. is added methyl chloroacetimidate hydrochloride [prepared according to procedures described by R. Rogers and D. G. Nielson, Chem. Rev., 61, 179 (1961)](8.6 g). The reaction is allowed to warm to room temperature while stirring overnight. The mixture is washed with water three times; dried over magnesium sulfate and concentrated to an oil. The oil is distilled (120°-135° C. at 0.5 mm Hg) to give 7.8 g (71% yield) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04675405 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-465ec160f50a4058b62cc6962c2f5f66 |
| Source note | uspto-grants-1987_06 |