HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → (S)-4-benzyloxy-1-trityloxy-2-butanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (S)-4-Benzyloxy-1,2-butanediol | HCID 9794180 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-4-benzyloxy-1-trityloxy-2-butanol | HCID 11015650 | 100% |
Reaction Steps
In toluene (100 ml) were dissolved (S)-4-benzyloxy-1,2-butanediol (25.8 g, 0.132 mol), triethylamine (20.2 ml, 0.145 mol) and 4-N,N-dimethylaminopyridine (DMAP) (0.80 g, 6.58 mmol). After cooling in ice bath, trityl chloride (36.69 g, 0.1316 mol) was added to the solution and the mixture was stirred at room temperature for 10 hours. The mixture was condensed in vacuo, diluted with ethyl acetate, washed with water and then saturated brine, dried on sodium sulfate, filtered and condensed in vacuo to give (S)-4-benzyloxy-1-trityloxy-2-butanol quantitatively (55.89, yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06620977B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-f1587c997a9841998fb1cbfc8baf52ff |
| Source note | uspto-grants-2003_09 |