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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 130801Generated: November 1, 2026

Ethyl Acetate → Methoxy-3-methyl-1,3,4,5-tetrahydrobenzo[d]azepin-2-one

https://huagongshe.com/reaction/130801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant8-methoxy-3-methyl-2,3-dihydro-1H-3-benzazepin-2-oneHCID 59730294—
CatalystPalladiumHCID 23938—
ProductMethoxy-3-methyl-1,3,4,5-tetrahydrobenzo[d]azepin-2-oneHCID 6874921393%

Reaction Conditions

Temperature25 °C

Reaction Steps

Weigh out 5% Pd on carbon (100 g) to a suitable container and wet the catalyst with ethyl acetate (2 L) while maintaining a nitrogen blanket. Charge the catalyst slurry to a 10-gallon autoclave and rinse the container with ethyl acetate (1 L) while maintaining a nitrogen purge. Add 8-methoxy-3-methyl-1,3-dihydrobenzo[d]azepin-2-one (920 g, 4.5 mol) to the autoclave and rinse with ethyl acetate (4 L). Purge the autoclave with nitrogen, seal the autoclave and pressurize with hydrogen to 50 psi while stirring at 800 rpm and maintaining the reaction temperature between 20-30° C. The reaction is determined to be complete by 1H NMR after 5 hours. Filter the autoclave contents over hyflo and rinse with ethyl acetate, then concentrate the filtrate to obtain the product methoxy-3-methyl-1,3,4,5-tetrahydrobenzo[d]azepin-2-one as an off-white solid (868 g, 93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07381719B2
Source datasetuspto-grants-2008_06
ORD IDord-400a6a342db94e568b66773a8b359beb
Source noteuspto-grants-2008_06