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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415115Generated: October 30, 2026

HCID 69856072, compound → HCID 22639973, compound

https://huagongshe.com/reaction/2415115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69856072HCID 69856072—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22639973HCID 22639973—

Reaction Steps

To a solution of 600 mg (1.1 mmol) of 2-methyl-butyric acid 8-(2-[1-(3,4-dimethyoxy-benzyl)-4-hydroxy-6-oxopiperidin-2-yl]-ethyl)-3,7-dimethyl-1,2,3,7,8,8a-hexahydro-naphthalen-1-yl ester in 15 ml of THF at rt are added 2 ml of a 65% RedAl® solution in toluene. After 3 hours, the reaction is quenched by the addition of 1 ml of methanol. The organic phase is extracted twice with 15 ml of 2N HCl. The aqueous phases are combined, brought to pH 12 with 1N NaOH and extracted three times with ethyl acetate. The organic phases are combined, dried over sodium sulfate and the solvent evaporated. The residue is purified by silica gel chromatography (t-butyl methyl ether/methanol 9/1) to afford pure 1-(3,4-Dimethoxy-benzyl)-2-[2-(8-hydroxy-2,6-dimethyl-1,2,6,7,8,8a-hexahydro-naphthalen-1-yl)-ethyl]-piperidin-4-ol as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818638B2
Source datasetuspto-grants-2004_11
ORD IDord-f60075df249d45f893eb8cfcf5e1ab95
Source noteuspto-grants-2004_11