HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → HCID 23041821, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 13922713 | HCID 13922713 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 23041821 | HCID 23041821 | 6.8% |
Reaction Steps
78 g (0.28 mol) of tert.-butyl Z-2-(2-acetamidothiazol-4-yl)but-2-enoate are suspended in a mixture of 2 l of carbon tetrachloride and 15 ml of glacial acetic acid at 0° C. 43 g (0.32 mol) of sulphuryl chloride, dissolved in 600 ml of carbon tetrachloride, are added dropwise in the course of five hours, while stirring. The solution is extracted once with saturated sodium bicarbonate solution and once with water, dried and concentrated to about 200 ml. The product which has precipitated is filtered off with suction and washed with ether (53.4 g). The mother liquor is evaporated completely and a second fraction of the product (6 g) is obtained by crystallization of the residue with ether/ligroin. Yield: 59.4 g=67.8% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04943568 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-930e4db8fe0c417d9a467f71eb6d1e03 |
| Source note | uspto-grants-1990_07 |