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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706256Generated: October 31, 2026

HCID 20337419, compound → HCID 20337479, compound

https://huagongshe.com/reaction/1706256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20337419HCID 20337419—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
ProductHCID 20337479HCID 20337479—

Reaction Steps

A 1 N ethereal solution of butyllithium (9 ml.) is added with stirring, under a nitrogen atmosphere to a suspension of 3.57 g. (10 mmoles) of methyltriphenylphosphonium bromide (prepared from methyl bromide and triphenylphosphine) in 50 ml. of ether. 5,6,7,8,9,10-Hexahydro-2-hydroxy-3-(1-methyl-4-phenylbutyl)-6,6-dimethyl-10-oxo-benzo[c]quinoline (600 mg., 1.5 mmoles) dissolved in 100 ml. of ether is added and the mixture is stirred for four hours then allowed to stand overnight at room temperature. Ether is distilled off as tetrahydrofuran is added until most of the ether is replaced. The mixture was then refluxed for six hours, cooled and worked-up as described in Part A of Example 42 to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206225
Source datasetuspto-grants-1980_06
ORD IDord-cad08746bf69492097e922831dc792d1
Source noteuspto-grants-1980_06