HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → Ethyl 5-nitro-1,2-benzisothiazole-3-acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ethyl alpha-cyano-5-nitro-1,2-benziso-thiazole-3-acetate | HCID 12607115 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 5-nitro-1,2-benzisothiazole-3-acetate | HCID 18314495 | 17.1% |
Reaction Steps
Ethyl α-cyano-5-nitro-1,2-benzisothiazole-3-acetate (6.67 g, 0.0229 mol) is added to a solution of acetyl chloride (67.0 mL) in ethanol. The reaction mixture is refluxed overnight, cooled, and filtered to remove solids. The resultant filtrate is concentrated in vacuo to obtain a brown semi-solid. A mixture of the semi-solid in diethyl ether is stirred for two hours and filtered to obtain a solid. The solid is washed with diethyl ether and air-dried to give the title product as yellow crystals (1.04 g, mp 91-92° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06313295B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-2d2880cf5adf4c7ab447c2bdf27ffa6f |
| Source note | uspto-grants-2001_11 |