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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827308Generated: October 31, 2026

Acetic Acid → 3-Amino-2,3,4,5-tetrahydro-1H-benzazepin-2-one

https://huagongshe.com/reaction/1827308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 73866833HCID 73866833—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-Amino-2,3,4,5-tetrahydro-1H-benzazepin-2-oneHCID 443443367.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

5 g (26,3 mmol) of 4,5-dihydro-1H-benzo[b]azepine-2,3-dione 3-oxime is taken in 50 ml of methanol then 6,3 g (105 mmol) acetic acid is added. The reaction mixture is left to stir at 50° C. and 5 bar hydrogen pressure for 21 hours in the presence of 1,1 g Pd catalyst (5% on charcoal, containing 50% water). The reaction mixture is evaporated after filtration and the residue is dissolved in 16,5 ml water. 9,5 ml dichloromethane is added and the pH value is adjusted to pH 12–14 with NaOH (32%). After phase separation the aqueous layer is extracted two times with 5,5 ml dichloromethane each. The organic phases are dried over sodium sulfate and evaporated to give 3,12 g 3-amino-1,3,4,5-tetrahydro-benzo[b]azepin-2-one, yield 67,4%, HPLC 94,5 area %, RT=2.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053211B2
Source datasetuspto-grants-2006_05
ORD IDord-d93c5712be93439d914febf7087dd604
Source noteuspto-grants-2006_05