HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 3-Triphenylmethoxy-1-octyne
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Bromotriphenylmethane | HCID 11692 | — |
| Reactant | 1-Octyn-3-ol | HCID 13166 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Triphenylmethoxy-1-octyne | HCID 12675347 | — |
Reaction Steps
A mixture of 1.26 g. (10.0 mmoles) of 1-octyn-3-ol, 4.85 g. (15.0 mmoles) of triphenylmethyl bromide, and 50 ml. of dry pyridine is heated at 95° C. for 60 minutes with occasional swirling. The solution is cooled, treated with water, and extracted with ether. The extact is washed successively with water and saturated sodium chloride solution, dried over magnesium sulfate, and concentrated. The crude product is purified by chromatography on Florisil and recrystallization from petroleum ether to give white crystals, m.p. 65°-66.5°,δmax. (KBr) 3280 (acetylenic hydrogen), 1605, 1030, and 702 cm-1 (triphenylmethoxy group).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04007210 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-7f75aff0e2a74e5cb323650d9e819282 |
| Source note | uspto-grants-1977_02 |