HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 4158166, compound → 2-(Chloroethynyl)-5-nitrofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 4158166 | HCID 4158166 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-(Chloroethynyl)-5-nitrofuran | HCID 21434741 | — |
Reaction Steps
To a stirred solution of 20.8 g of 1 in 100 ml of dry tert-butanol was added dropwise at 5°-10° over a 30-minute period a solution of 11.2 g of potassium tert-butoxide in 100 ml of tert-butanol. The mixture then was stirred at 5°-10° for 1 hour longer. Concentration of the mixture under reduced pressure gave a dark residue which was extracted with ether and water. The ether phase was separated, dried over magnesium sulfate and Claisen distilled to give 4 as a liquid, b.p.: 73°-76° at 0.2 torr which solidified on standing, the solid having a melting point of 38°-41°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04024161 |
| Source dataset | uspto-grants-1977_05 |
| ORD ID | ord-be08813211e54a99922aeac92e8742b8 |
| Source note | uspto-grants-1977_05 |