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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625927Generated: October 30, 2026

Water → 1-Benzyl-8-methoxy-2,3,4,5-tetrahydro-1H-benzo[C]azepine

https://huagongshe.com/reaction/625927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-Benzyl-8-methoxy-4,5-dihydro-1H-benzo[C]azepin-3(2H)-oneHCID 70982269—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-8-methoxy-2,3,4,5-tetrahydro-1H-benzo[C]azepineHCID 7098217569%

Reaction Steps

To a solution of 2.17 mmol of 1-benzyl-8-methoxy-4,5-dihydro-1H-benzo[c]azepin-3(2H)-one in tetrahydrofuran under nitrogen atmosphere was added 3.25 mmol of lithiumaluminumhydride as 1 M solution in tetrahydrofuran. The solution was heated to reflux and stirred for 1.5 h. The mixture was cooled to room temperature and water (1 ml) was carefully added. The mixture was concentrated and the residue was dissolved in ethyl acetate. The organic phase was extracted with acidified water (acidified with 1 M HCl, 4×). To the combined aqueous phase was added NaOH (50%) until basic and ethyl acetate. The suspension was filtered over celite. The residue was washed with water and ethyl acetate. Phases were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over MgSO4 and filtered. Evaporation of the solvent gave 439 mg of crude material that was purified by flash chromatography to yield 399 mg of 1-benzyl-8-methoxy-2,3,4,5-tetrahydro-1H-benzo[c]azepine (69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309200B2
Source datasetuspto-grants-2016_04
ORD IDord-b6829b1e84ad4b3d87ea82d2e31441ea
Source noteuspto-grants-2016_04