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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586922Generated: October 31, 2026

HCID 22329264, compound → HCID 22329067, compound

https://huagongshe.com/reaction/586922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22329264HCID 22329264—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22329067HCID 2232906754.6%

Reaction Conditions

Temperature55 °C

Reaction Steps

In THF (10 ml) was dissolved t-butyl N-(4-bromo-2-formylphenyl)-N-cyclopropyl-4-aminobutyrate (1 g). To the solution was added potassium t-butoxide (0.59 g), and the mixture was heated at 55° C. for 1.5 hours. The solvent was evaporated, which was extracted with water. The aqueous layer was washed with ethyl acetate, and neutralized by addition of 1N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and dried with anhydrous magnesium sulfate. The solvent was evaporated to give 7-bromo-1-cyclopropyl-2,3-dihydro-1H-1-benzazepine-4-carboxylic acid (0.44 g) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936602B1
Source datasetuspto-grants-2005_08
ORD IDord-d056abadc9d64fcfa29329e5ad0d686b
Source noteuspto-grants-2005_08