HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Allyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy-]2-fluorobenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1-Adamantyl)-4-methoxybenzoyl chloride | HCID 10804497 | — |
| Reactant | Allyl 2-fluoro-4-hydroxybenzoate | HCID 14852522 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Allyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy-]2-fluorobenzoate | HCID 14852489 | 78.1% |
Reaction Steps
To a mixture of 1.96 g (10 mmoles) of allyl 2-fluoro-4-hydroxybenzoate, 1.53 ml (11 mmoles) of triethylamine and 25 ml of THF, there is slowly added a solution of 3 g (10 mmoles) of 3-(1-adamantyl)-4-methoxybenzoyl chloride in 50 ml of THF. The reaction medium is stirred at ambient temperature for 12 hours and then poured into water and extracted with ethyl ether. The organic phase is decanted, washed with water, dried on magnesium sulfate and evaporated. The resulting residue is purified by chromatography on a silica column, eluted by a 50:50 mixture of dichloromethane and hexane. After evaporation of the solvents, 3.63 g (78% yield) of the expected ester having a melting point of 102°-104° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05468897 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-d3a2396790a547aa89c7fa67fe94cbfc |
| Source note | uspto-grants-1995_11 |