HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2-(5-t-Butylthiophen-2-yl)-cyclopropanecarbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(5-t-Butylthiophen-2-yl)-cyclopropanecarboxylic acid | HCID 20139960 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(5-t-Butylthiophen-2-yl)-cyclopropanecarbonyl chloride | HCID 20139958 | 99% |
Reaction Steps
A mixture of 2-(5-t-butylthiophen-2-yl)-cyclopropanecarboxylic acid (3.38 g, 0.015 mol) and oxalyl chloride (2.65 g, 0.021 mol) in hexane (35 ml) was stirred at room temperature for 2 hours and then warmed at 60° C. for 3 hours. The hexane and excess oxalyl chloride were removed in vacuo to give 2-(5-t-butylthiophen-2-yl)-cyclopropanecarbonyl chloride (3.59 g, 99%) as a pale yellow liquid which was used in the next stage without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04743602 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-4e2b07b47cbc4f229417953df664b060 |
| Source note | uspto-grants-1988_05 |