HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 14054080, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | HCID 86745224 | HCID 86745224 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Product | HCID 14054080 | HCID 14054080 | — |
Reaction Steps
To a solution of 2.43 ml 0.0325 mol) but-2-yn-1-ol and 3.97 g (0.0325 mol of 4-dimethylaminopyridine in 35 ml tetrahydrofuran is added dropwise, at 0°-5° C., a solution of 7.95 g 0.0325 mol 2-(4-chlorophenyl-3,3-dimethylbutyryl chloride in 25 ml tetrahydrofuran. The reaction mixture was allowed to warm to room temperature and after one and a half hours worked up as follows: after removal of the tetrahydrofuran in vacuo, it was treated with water and stirred with ether, the ether phase was dried over magnesium sulphate and concentrated in vacuo. A colourless oil was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066675 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-055be7d36ea34b998a8f97432033e77c |
| Source note | uspto-grants-1991_11 |