HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyacetonitrile → Cyanomethyl thiophene-2-sulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyacetonitrile | HCID 7857 | — |
| Reactant | 2-Thiophenesulfonyl chloride | HCID 85518 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cyanomethyl thiophene-2-sulfonate | HCID 20556342 | — |
Reaction Steps
Method of preparation: Glycolonitrile is reacted with 2-thiophenesulfonyl chloride using the procedure as described in the previous example, with 2 hours of reaction at 0° C., followed by three hours at room temperature. The reaction mixture separates into two layers; the bottom dark layer is isolated and dissolved in diethyl ether, the solution washed with weak caustic solution and cold water, and the solvent is stripped off under reduced pressure to give the product (in 79% conversion), a green oily liquid, nD24.5 1.535.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04029809 |
| Source dataset | uspto-grants-1977_06 |
| ORD ID | ord-022c477181ea4de59e8ceadaf7dfd2ed |
| Source note | uspto-grants-1977_06 |