HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butanol → HCID 69926284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 22674259 | HCID 22674259 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69926284 | HCID 69926284 | 357.2% |
Reaction Steps
To a solution of 1.90 g (6.88 mmol) 2-methylsulfanyl-4-o-tolyloxy-pyrimidine-5-carboxylic acid, 0.95 ml triethylamine (6.88 mmol) and 1.29 ml (1.37 mmol) t-butanol in 25 ml THF, 1.47 ml (6.88 mmol) diphenylphosphorylazide were added and the resulting solution heated at reflux for 12 hrs. After evaporation of the solvent, the residue was distributed between CH2Cl2 and H2O. The aquoeus phase was extracted twice with 80 ml CH2Cl2. The combined organic layers were dried (Na2SO4), filtered and evaporated. The residue was purified by chromatography (SiO2, CH2Cl2, ethyl acetate 40:1) to give 1.70 g (71%) (2-methylsulfanyl-4-o-tolyloxy-pyrimidin-5-yl)-carbamic acid tert.-butyl ester as a colorless solid, MS (ISP): 348.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06787539B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-5c566e7128214bab9b9191cbd2f9bcb2 |
| Source note | uspto-grants-2004_09 |