HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Allyl 4-[3-(1-adamantyl)-4-methoxyethoxymethoxybenzamido]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Prop-2-en-1-yl 4-aminobenzoate | HCID 13075143 | — |
| Reactant | 3-(1-Adamantyl)-4-methoxyethoxymethoxybenzoyl chloride | HCID 57233102 | — |
| Solvent | Water | HCID 962 | — |
| Product | Allyl 4-[3-(1-adamantyl)-4-methoxyethoxymethoxybenzamido]benzoate | HCID 67663874 | — |
Reaction Steps
700 mg (3.95 mmol) of allyl 4-aminobenzoate, 1 ml (4.3 mmol) of triethylamine and 50 ml of THF were introduced into a round-bottomed flask. A solution of 1.5 g (3.96 mmol) of 3-(1-adamantyl)-4-methoxyethoxymethoxybenzoyl chloride was added dropwise and the mixture was stirred at room temperature for 4 hours. The reaction medium was poured into water and extracted with ethyl ether. The organic phase was separated out after settling had taken place, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a column of silica, eluted with dichloromethane. 1.7 g (83%) of the expected allylic ester was recovered in the form of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05786379 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-b46855fa87a44f10b58563b1917e71b5 |
| Source note | uspto-grants-1998_07 |