HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 52951165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 10043064 | HCID 10043064 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 52951165 | HCID 52951165 | 62% |
Reaction Steps
To a solution of acid 4 (0.74 g, 2 mmol) in 10 mL of EtOH and 10 mL of 1,4-dioxane was added diphenylphosphonylazide (0.52 mL, 2.4 mmol) followed by Et3N (0.34 mL, 2.4 mmol). The reaction mixture was refluxed overnight. After cooling the reaction mixture to room temperature, EtOAc and water were added. The organic layer was separated, washed with brine, dried over MgSO4 and concentrated in vacuo. The residue was purified by column chromatography to give the titled compound (0.48 g, 62%) as a white solid. mp 120.9-127.5° C. 1H NMR (300 MHz, DMSO-d6): δ 10.30 (s, 1H), 7.79 (d, J=8 Hz, 2H), 7.50-7.34 (m, 7H), 7.33-7.25 (m, 2H), 6.74 (s, 1H), 4.14 (q, J=7 Hz, 2H), 1.24 (t, J=7 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09096532B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-bec77657c8f5422fac0ddafbccccf586 |
| Source note | uspto-grants-2015_08 |