HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Benzyl-piperidin-4-yl 2-methoxy-benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzylpiperidin-4-ol | HCID 78461 | — |
| Reactant | 2-Methoxybenzoyl chloride | HCID 88969 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Benzyl-piperidin-4-yl 2-methoxy-benzoate | HCID 18919786 | 69% |
Reaction Steps
1.41 g (0.00733 mol) of 1-benzyl-4-hydroxypiperidine and 1.8 ml (0.0129 mol) of triethylamine were dissolved in 50 ml of toluene and treated with 0.79 ml (0.00586 mol) of 2-methoxy-benzoyl chloride. The mixture was boiled at reflux for 2 hrs., the precipitate was filtered off and the filtrate was concentrated. The residue was chromatographed over silica gel with ethyl acetate/hexane (1:2). 1.31 g (69%) of 1-benzyl-piperidin-4-yl 2-methoxy-benzoate were obtained as a yellowish oil. MS: me/e=326 (C20H24NO3 +).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753679 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-0cd03ccf5b6c4bdf9ce9ae0f7e0f9d26 |
| Source note | uspto-grants-1998_05 |