HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → Methyl 3-(acetyloxy)thiophene-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 54299211 | HCID 54299211 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 3-(acetyloxy)thiophene-2-carboxylate | HCID 12593664 | 79% |
Reaction Steps
20.2 Parts of 3-acetoxydihydrothiophene-2-carboxylic acid methyl ester are reacted with 6.75 parts by volume of sulfuryl chloride in 150 parts by volume of CCl4 at 0° C. for one hour. The end product is isolated from the reaction mixture by the method described in Example 14c). 15.8 parts (79% of theory) of 3-acetoxythiophene-2-carboxylic acid methyl ester of boiling point 84°-86° C./0.04 mbar are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04239897 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-128db0d46f9a49418b703e9cb483d14c |
| Source note | uspto-grants-1980_12 |