HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (6-Phenoxy-2-pyridyl)methyl 2-(2-napthyl)-3-methyl-butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Phenoxy-2-pyridinemethanol | HCID 12879155 | — |
| Reactant | 3-Methyl-2-(naphthalen-2-yl)butanoic acid | HCID 13952228 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (6-Phenoxy-2-pyridyl)methyl 2-(2-napthyl)-3-methyl-butanoate | HCID 23341821 | — |
Reaction Steps
To a stirred solution of (6-phenoxy-2-pyridyl)methanol (0.2 g, 0.99 mmol) and triethylamine (0.14 g, 1.38 mmol) in ether (about 15 ml), under nitrogen, is added by syringe a solution of the acid chloride of 2-(2-naphthyl)-3-methylbutanoic acid (1.5 mmol) in ether. The mixture is stirred for 30 minutes and then quenched with saturated aqueous sodium bicarbonate. The ether phase is washed with aqueous sodium bicarbonate, water and brine and filtered through silica. Evaporation of solvent, followed by thin layer chromatography using a circular chromatograph, eluting with 20% ether/hexane, gives (6-phenoxy-2-pyridyl)methyl 2-(2-napthyl)-3-methyl-butanoate, MS m/e 411(M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04223033 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-21ee06759d834d7491dd59f80584af11 |
| Source note | uspto-grants-1980_09 |