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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 8-methoxy-3-methyl-2,3-dihydro-1H-3-benzazepin-2-one | HCID 59730294 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | Methoxy-3-methyl-1,3,4,5-tetrahydrobenzo[d]azepin-2-one | HCID 68749213 | 93% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07381719B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-400a6a342db94e568b66773a8b359beb |
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| Source note | uspto-grants-2008_06 |
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