HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 4-trityloxybutan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-trityloxybutan-1-ol | HCID 371702 | 41.6% |
Reaction Steps
To a solution of 45 g of butane-1,4-diol in 0.25 of pyridine, cooled to 0° C., were added 139.4 g of triphenylchloromethane and the mixture was stirred at room temperature for 26 h. The precipitate formed was removed by filtration and the filtrate was evaporated in vacuo. The residue was taken up in 0.5 l of ethyl acetate and the solution was washed successively with 200 ml portions of water, 1N hydrochloric acid, water, 5% sodium bicarbonate solution and brine. The organic layer was dried over sodium sulfate and evaporated in vacuo. Crystallization of the residual material from ethyl acetate/hexane afforded 69.0 g of 4-trityloxy-1-butanol as white crystals of m.p. 73°-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05594135 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-e9af9902f91548aa823d4c01ddcf9eaa |
| Source note | uspto-grants-1997_01 |