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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261446Generated: November 2, 2026

N-Methylformanilide → HCID 20394938, compound

https://huagongshe.com/reaction/261446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylformanilideHCID 66737—
ReactantHCID 13187661HCID 13187661—
ReactantButyllithiumHCID 178418339—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 20394938HCID 20394938—

Reaction Steps

A mixture of 7.8 g (0.0225 mole) of 6-bromo-7,8-methylenedioxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine in toluene was added to a mixture of 2.2 ml (6.07 mole) of butyl lithium diluted with 100 ml of ethyl ether at -78°. Then, 10 ml of N-methylformanilide was added. After stirring for 1 hour at -78°, the cooling bath was removed and 100 ml of 10% hydrochloric acid was added. After stirring for 15 minutes, the layers were separated. The ether layer was dried and evaporated. The residue was dissolved in ethyl acetate then extracted by aqueous sodium bisulfite. The aqueous layer was removed, washed with ether and made basic with solid carbonate. After extraction with ethyl ether the extracts were evaporated. The residue was heated in 6 N hydrochloric acid for 1 hour. The solution was made basic and the product extracted into chloroform. After purification over silica with 5% methanol-chloroform, 6-formyl-7,8-methylenedioxy-1-phenyl-2,3,4,5-tetrahydro- 1H-3-benzazepine was obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04165372
Source datasetuspto-grants-1979_08
ORD IDord-2b6345addc564aa0b812f4028ee98aff
Source noteuspto-grants-1979_08