HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 131729739, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | Toluene tert-butyl alcohol | HCID 22595558 | — |
| Reactant | HCID 68975739 | HCID 68975739 | — |
| Product | HCID 131729739 | HCID 131729739 | — |
Reaction Steps
To a mixture of Example 14, N4 in tert-BuOH:toluene (1:1, 0.171 M) was added diphenyl phosphoryl azide (2.2 eq) and Et3N (2.2 eq). The reaction was heated at reflux until consumption of the starting material and then volatiles were removed under reduced pressure. The resulting residue was partitioned between DCM and sat. aq. NaHCO3; the organic phase was separated, dried (Na2SO4) and filtered. Evaporation of the solvent provided yellow oil (O1) which was used as such in the next step without purification. MS (ES) C18H22FN3O3 required: 347. found: 348 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08188084B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-47ed9e902409445db5e27b7552b6ae10 |
| Source note | uspto-grants-2012_05 |