HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → 2-(5-t-Butylfuran-2-yl)-cyclopropanecarbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(5-t-Butylfuran-2-yl)-cyclopropanecarboxylic acid | HCID 20139962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(5-t-Butylfuran-2-yl)-cyclopropanecarbonyl chloride | HCID 20139947 | 101.2% |
Reaction Steps
A mixture of 2-(5-t-butylfuran-2-yl)-cyclopropanecarboxylic acid (3.6 g, 0.017 mol) and oxalyl chloride (4.4 g, 0.035 mol) in hexane (40 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-butylfuran-2-yl)-cyclopropanecarbonyl chloride (3.9 g, 100%) 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-d08a45b09c16472e88b16f654b30e951 |
| Source note | uspto-grants-1988_05 |