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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253736Generated: November 2, 2026

Benzaldehyde → 1-Benzyl-hexahydro-4H-azepin-4-one

https://huagongshe.com/reaction/1253736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAzepan-4-oneHCID 1501891—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventDichloromethaneHCID 6344—
Product1-Benzyl-hexahydro-4H-azepin-4-oneHCID 151435078%

Reaction Steps

To a suspension of azepan-4-one (8.0 g, 53.47 mmol, 1.0 eq.) in methylene chloride (100 ml) was added TEA followed by benzaldehyde and reaction mixture was stirred at RT for 30 min. Na(OAc)3BH was added portionwise to the reaction mixture and it was then stirred at RT for another 4 h. The reaction mixture was quenched with NaOH (2 M, 80 ml) and extracted with methylene chloride (3×100 ml). The organic layer was dried over Na2SO4 and solvent was evaporated under reduced pressure to afford the crude product which was purified by column chromatography (silica gel, 20% EtOAc/hexanes) to yield the desired product as an oil. Yield: 78% (8.5 g, 41.87 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455475B2
Source datasetuspto-grants-2013_06
ORD IDord-51a91f3063da46ff8a27b11bfc855e5c
Source noteuspto-grants-2013_06