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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228256Generated: October 27, 2026

Aluminium lithium hydride → methoxy-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine

https://huagongshe.com/reaction/228256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethoxy-3-methyl-1,3,4,5-tetrahydrobenzo[d]azepin-2-oneHCID 68749213—
SolventTetrahydrofuranHCID 8028—
SolventEther tetrahydrofuranHCID 21868444—
Productmethoxy-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepineHCID 687483421,028.5%

Reaction Steps

Dissolve methoxy-3-methyl-1,3,4,5-tetrahydrobenzo[d]azepin-2-one (375 g, 183 mmol, 1.0 eq) in THF (2.5 L) and add the solution via an addition funnel over 1 hour to slurry of lithium aluminium hydride (LAH) (175 g, 457 mmol, 2.5 eq) in ether/THF (4.5 L/2 L) in a 22 L reaction vessel under nitrogen while cooled in an ice/acetone bath. Add the starting amide at a rate to maintain the reaction temperature below 30° C. Stir the resulting mixture for 3 hours at room temperature under nitrogen. The reaction is determined to be complete by TLC. Cool the reaction mixture in an ice/acetone bath and quench slowly over 2 hours (off-gassing, exothermic) with water (175 mL) and 5.0 N NaOH solution (350 mL) added in succession. Filter the slurry and wash the solids with THF. Add sodium sulfate to the filtrate to remove any excess water, and then filter. Concentrate the filtrate down under vacuum to a dark oil to obtain the product methoxy-3-methyl-2,3,4,5-tetrahydro-1H-benzo[d]azepine (360 g, quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560463B2
Source datasetuspto-grants-2009_07
ORD IDord-01d29f776a444f8ca05f789c9d7b853c
Source noteuspto-grants-2009_07