HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 1,1',1''-{[(Hex-5-yn-3-yl)oxy]methanetriyl}tribenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | 5-Hexyn-3-ol | HCID 89223 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,1',1''-{[(Hex-5-yn-3-yl)oxy]methanetriyl}tribenzene | HCID 20565106 | — |
Reaction Steps
A stirred solution of 9.81 g. (0.10 moles) of 4-hydroxy-1-hexyne and 33.5 g. (0.12 moles) of triphenylmethyl chloride in 100 ml. of dry pyridine is heated at reflux for 2 hours. The cooled mixture is treated with water and extracted with a hexane-ether mixture. The extract is washed successively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. Column chromatography of the residue on Florisil gives an oil, ν max. 3290 (acetylenic hydrogen), 1600, 1030, and 705 cm-1 (triphenylmethoxy group).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04061672 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-50405bff5e8e4058a9c73da738b637a4 |
| Source note | uspto-grants-1977_12 |