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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111393Generated: October 30, 2026

Water → 8-Amino-6-methoxy-4-methyl-5-(8-phenyloctoxy) quinoline

https://huagongshe.com/reaction/1111393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantButyl etherHCID 8909—
Reactant6-Methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinolineHCID 54345436—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product8-Amino-6-methoxy-4-methyl-5-(8-phenyloctoxy) quinolineHCID 5439482961.1%

Reaction Steps

A stirred mixture of 6-methoxy-4-methyl-8-nitro-5-(8-phenyloctoxy) quinoline (2.1 g, 0.005 mol), degreased 40 mesh Fe filings (5 g), H2O (20 ml), HOAc (4 ml) and n-Bu2O (4 ml) was heated at 80° C. to 1.5 h, cooled and filtered. The solid was thoroughly extracted with Et2O and the filtered extract was dried (Na2SO4), treated with carbon and concentrated to an oil. Trituration with pet ether gave 1.2 g (61%) of 8-amino-6-methoxy-4-methyl-5-(8-phenyloctoxy) quinoline as yellow-green solid, mp 33°-34° C. Crystallization from pet ether (Darco) gave the analytical sample as yellow green crystals, mp 39°-40° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980360
Source datasetuspto-grants-1990_12
ORD IDord-e1e3b54f1b014628bc2b82556250e010
Source noteuspto-grants-1990_12