HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565665Generated: October 28, 2026
Potassium Carbonate → Tert-butyl [2-[2-[4-(diphenylmethoxy)-1-piperidinyl]ethyl]-2,3-dihydro-2,4,6,7-tetramethylbenzofuran-5-yl]carbamate
https://huagongshe.com/reaction/565665
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzhydryloxypiperidine | HCID 3017584 | — |
| Reactant | Tert-butyl [2-(2-bromoethyl)-2,3-dihydro-2,4,6,7-tetramethylbenzofuran-5-yl]carbamate | HCID 54438432 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl [2-[2-[4-(diphenylmethoxy)-1-piperidinyl]ethyl]-2,3-dihydro-2,4,6,7-tetramethylbenzofuran-5-yl]carbamate | HCID 53977860 | 92% |
Reaction Steps
A suspension of tert-butyl [2-(2-bromoethyl)-2,3-dihydro-2,4,6,7-tetramethylbenzofuran-5-yl]carbamate (1.2 g), 4-(diphenylmethoxy)piperidine (0.85 g), and potassium carbonate (0.44 g) in N,N-dimethylformamide (20 mL) was stirred at 60° C. for 15 hours. This reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with saturated aqueous NaCl, dried over MgSO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methanol=98:2 to 95:5) to provide 1.6 g of the title compound. Yield 92%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172085B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-c84db3e3158b48c6994c1892346494d0 |
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| Source note | uspto-grants-2001_01 |
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