HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(Benzocyclobuten-1-ylmethyl)-4-(2,4-difluorobenzoyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (2,4-Difluorophenyl)(piperidin-4-yl)methanone | HCID 13076388 | — |
| Reactant | Benzocyclobuten-1-ylmethyl para-toluenesulfonate | HCID 19886368 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(Benzocyclobuten-1-ylmethyl)-4-(2,4-difluorobenzoyl)piperidine | HCID 19886357 | — |
Reaction Steps
0.0019 mole of 4-(2,4-difluorobenzoyl)piperidine, 0.0019 mole of benzocyclobuten-1-ylmethyl para-toluenesulfonate and 0.04 mole of triethylamine dissolved in 50 ml of toluene are mixed and then brought to reflux for 18 hours. The reaction medium is then extracted with 1N hydrochloric acid and the aqueous phase is alkalinized and extracted with dichloromethane. The oil obtained is purified on a silica column using a mixture of cyclohexane and acetone (93:7 V/V) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05100902 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-f5eb0bff7d204453aad3f54dba98b3d2 |
| Source note | uspto-grants-1992_03 |