HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253989Generated: October 30, 2026
Benzylamine → 6-Benzyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepine
https://huagongshe.com/reaction/253989
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Di(2-methanesulfonyloxyethyl)furan | HCID 86602387 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Benzyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepine | HCID 19600185 | — |
Reaction Steps
A solution of 2,3-di(2-methanesulfonyloxyethyl)furan (114 mmol) in dioxane (168 mL) is treated with potassium carbonate (337 mmol) and benzyl amine (70.1 mmol) and heated to 102° C. for 18 hours. The reaction is cooled, the precipitate removed by filtration, and the mother liquor concentrated to give a crude oil which is purified by silica chromatography (EtOAc/hexanes eluant) to provide 6-benzyl-5,6,7,8-tetrahydro-4H-furo[3,2-d]azepine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07872031B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-3f0a9d1a984b4a5cb57e699822504956 |
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| Source note | uspto-grants-2011_01 |
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