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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844602Generated: November 4, 2026

Stannous chloride dihydrate → 5-Tert-butyl-2-methoxy-3-methylsulphanylmethyl-aniline

https://huagongshe.com/reaction/1844602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
Reactant5-Tert-butyl-2-methoxy-1-methylsulphanylmethyl-3-nitro-benzeneHCID 58493925—
SolventEthanolHCID 702—
Product5-Tert-butyl-2-methoxy-3-methylsulphanylmethyl-anilineHCID 67216913—

Reaction Steps

A mixture of 1.00 g 5-tert-butyl-2-methoxy-1-methylsulphanylmethyl-3-nitro-benzene, 4.20 g tin dichloride dihydrate and 15 ml of ethanol is refluxed for 2 h. Then the solvent is removed, and water and dichloromethane are added to the residue. The mixture is filtered through Celite, and the aqueous part of the filtrate is separated off and extracted twice with dichloromethane. The combined organic phases are dried (Na2SO4), and the solvent is removed. The residue is chromatographed on aluminium oxide with cyclohexane/ethyl acetate (4:1→1:4) as eluant.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946438B2
Source datasetuspto-grants-2015_02
ORD IDord-c218c5992d374d66bf32430666fce0aa
Source noteuspto-grants-2015_02