HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-(Chloromethyl)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | 2-Chloro-1,1,1-triethoxyethane | HCID 305922 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Chloromethyl)benzothiazole | HCID 304978 | 91.3% |
Reaction Steps
A solution of 2-chloro-1,1,1-triethoxyethane (5.9 g) and 2-aminothiophenol (2.5 g) was heated at 80° C. for 15 minutes. After cooling to room temperature, it was dissovled in methylene chloride (30 ml) and the resulting solution was washed with 3N HCl (10 ml) and then with water (20 ml). The organic portion was evaporated and the residue chromatographed over silica gel to obtain 2-chloromethylbenzothiazole (3.35 g; 90% yield), m.p. 34° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04723010 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-7628ca281c8a4d939d7e63b118d19a45 |
| Source note | uspto-grants-1988_02 |