HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → tert-butyl-7-[3-(5-Methyl-2-phenyl-4-oxazolyl)propoxy]chromane-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(5-Methyl-2-phenyl-1,3-oxazol-4-yl)propyl methanesulfonate | HCID 22087833 | — |
| Reactant | Tert-butyl 7-hydroxychromane-3-carboxylate | HCID 59832111 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-butyl-7-[3-(5-Methyl-2-phenyl-4-oxazolyl)propoxy]chromane-3-carboxylate | HCID 69279614 | — |
Reaction Steps
To a stirred solution of tert-butyl 7-hydroxychromane-3-carboxylate (250 mg, 1 mmol) in CH3CN (10 ml), K2CO3 (414 mg) and 3-(5-methyl-2-phenyl-1,3-oxazol-4-yl)propyl methanesulfonate (325 mg) were added and the reaction mixture was heated under reflux for overnight. The reaction mixture was cooled to room temperature and diluted with 30 mL of diethyl ether. The diluted solution was passed through a pad of silica and the silica was washed with more ether. The ether solution was evaporated to dryness and purified using silica chromatography. The product was isolated as a white sold (397 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446127B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-f4b3c15d976d4c24b6e3b2b89e5cb375 |
| Source note | uspto-grants-2008_11 |