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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111390Generated: October 30, 2026

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

https://huagongshe.com/reaction/1111390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantButyl etherHCID 8909—
Reactant6-Methoxy-4-methyl-8-nitro-5-[4-phenylbutoxy]quinolineHCID 563517—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product8-Amino-6-methoxy-4-methyl-5-(4-phenylbutoxy)quinolineHCID 60914566%

Reaction Steps

A stirred mixture of 6-methoxy-4-methyl-8nitro-5-(4-phenylbutoxy) quinoline (3.7 g, 0.01 mol), degreased 40mesh Fe filings (10 g), H2O (40 ml), HOAc (8 ml) and Bu2O (8 ml) was heated at 80°-100° C. for 2.5 h, allowed to cool and filtered. The solid was thoroughly extracted with Et2O and the extract was dried (Na2SO4), treated with carbon and concentrated to an oil. Extraction of the latter with pet ether and cooling the extract gave 2.2 g (66%) of 8-amino-6methoxy-4-methyl-5-(4-phenylbutoxy)quinoline as yellow-green crystals, mp 59°-59.5° C. Recrystallization from pet ether afforded the analytical sample as yellow crystals, mp 60°-61° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980360
Source datasetuspto-grants-1990_12
ORD IDord-e1e7ddb3fc28425cb074cde3b859a77e
Source noteuspto-grants-1990_12