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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648941Generated: October 30, 2026

Sodium hydride → Butyl 3-amino-6-benzyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepine-2-carboxylate

https://huagongshe.com/reaction/1648941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantButyl GlycolateHCID 81882—
Reactant1-Benzyl-4-chloro-5-cyano-2,3,6,7-tetrahydro-1H-azepineHCID 13072032—
Solvent1,4-DioxaneHCID 31275—
ProductButyl 3-amino-6-benzyl-5,6,7,8-tetrahydro-4H-furo[2,3-d]azepine-2-carboxylateHCID 20481347—

Reaction Steps

A solution of 1.0 gm (0.008 mol) of butyl glycolate in 8 ml of absolute dioxane was added dropwise to a suspension of 0.4 gm (0.008 mol) of 50% sodium hydride in 5 ml of absolute dioxane, and the mixture was stirred for one hour at room temperature. Then, while the mixture was cooled with ice, a solution of 1.0 gm (0.004 mol) of 1-benzyl-4-chloro-5-cyano-2,3,6,7-tetrahydro-1H-azepine in 15 ml of absolute dioxane was added, and the mixture was stirred for one hour. The reaction mixture was then poured into about 80 ml of ice-cold water, and the aqueous mixture was extracted three times with ethyl acetate. The combined organic phases were washed twice with water, dried over sodium sulfate and concentrated by evaporation. The residue was purified by column chromatography on silicagel, using toluene/ethyl acetate (7:3) as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04414225
Source datasetuspto-grants-1983_11
ORD IDord-c641c795bc4f4bbb883ca4db35fce154
Source noteuspto-grants-1983_11