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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3-Di(2-methanesulfonyloxyethyl)furanHCID 86602387—
Solvent1,4-DioxaneHCID 31275—
Product6-Benzyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepineHCID 19600185—

Reaction Conditions

Temperature102 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872031B2
Source datasetuspto-grants-2011_01
ORD IDord-3f0a9d1a984b4a5cb57e699822504956
Source noteuspto-grants-2011_01