HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463855Generated: October 26, 2026
Potassium Carbonate → 2,2-diphenyl-5-[N-{2-(1,4-benzodioxan-6-yl)ethyl}-N-methylamino]pentanamide
https://huagongshe.com/reaction/1463855
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2-Diphenyl-5-methylaminopentanamide | HCID 19088475 | — |
| Reactant | 6-(2-Bromoethyl)-2,3-dihydro-1,4-benzodioxin | HCID 19088508 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,2-diphenyl-5-[N-{2-(1,4-benzodioxan-6-yl)ethyl}-N-methylamino]pentanamide | HCID 19088511 | — |
Reaction Steps
A mixture containing 2,2-diphenyl-5-methylaminopentanamide (0.36 g--see Preparation 1), 6-(2-bromoethyl)-1,4-benzodioxan (0.32 g), anhydrous potassium carbonate (0.75 g) and acetonitrile (20 ml) was heated under reflux for 16 hours. The mixture was partitioned between dichloromethane (50 ml) and 10% aqueous sodium carbonate (30 ml), the layers separated and the aqueous layer extracted with dichloromethane (3×20 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give an oil which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give a foam which was further purified by column chromatography on alumina eluting with dichloromethane containing methanol (0% up to 5%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as a foam, yield 0.11 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05302595 |
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| Source dataset | uspto-grants-1994_04 |
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| ORD ID | ord-5d488d55105d40e582504a4c8e2cbe42 |
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| Source note | uspto-grants-1994_04 |
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