HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(4-Hydroxy-3-thienyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 20300157 | HCID 20300157 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Hydroxy-3-thienyl)ethanone | HCID 21716 | 77% |
Reaction Steps
2.88 Parts of 3-hydroxy-4-acetyldihydrothiophene are introduced into 20 parts by volume of dried methylene chloride; a solution of 1.7 parts by volume of sulfuryl chloride in 20 parts by volume of dried methylene chloride is added in the course of 10 minutes at 0° C. During the reaction, nitrogen is passed in, in order to expel the hydrochloric acid formed. After 30 minutes, the reaction mixture is worked up. The end product is isolated from the reaction mixture by the method described in Example 1c. 2.22 parts (77% of theory) of 3-hydroxy-4-acetylthiophene of melting point 44°-47° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04239897 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-36eaf097a39d4d3783eee7580f8473d7 |
| Source note | uspto-grants-1980_12 |