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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290955Generated: October 25, 2026

N-Methylhomoveratrylamine → 3,4-Dichloro-N-[4-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]butyl]-N-(1-methylethyl)benzenesulfonamide

https://huagongshe.com/reaction/2290955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylhomoveratrylamineHCID 77039—
ReactantN-isopropyl-N-(4-oxobutyl)-3,4-dichlorobenzenesulfonamideHCID 13770967—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
Product3,4-Dichloro-N-[4-[[2-(3,4-dimethoxyphenyl)ethyl]methylamino]butyl]-N-(1-methylethyl)benzenesulfonamideHCID 13770968—

Reaction Steps

The aldehyde prepared in the preceding paragraph (8.90 g, 0.027 m) and N-methyl-homoveratrylamine (5.29 g, 0.027 m) in absolute ethanol (100 ml) containing PtO2 (0.6 g) was shaken under hydrogen (7 hours) and the reaction filtered and stripped to provide the crude product (13.32 g) as a dark greenish gum. This material was chromatographed, after removal of a small amount of insoluble solid, on dry column silica gel (500 g) with 30% methanol/70% ethyl acetate to provide the title compound (7.26 g) as a clear white gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04618711
Source datasetuspto-grants-1986_10
ORD IDord-fe203a9032f446659f56f459b8ba90a1
Source noteuspto-grants-1986_10