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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636491Generated: October 26, 2026

Water → 3-Amino-1-(tert-butyldiphenylsilyloxymethyl)-2,6-dimethylbenzene

https://huagongshe.com/reaction/636491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Tert-butyldiphenylsilyloxymethyl)-2,6-dimethyl-3-nitrobenzeneHCID 10764557—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product3-Amino-1-(tert-butyldiphenylsilyloxymethyl)-2,6-dimethylbenzeneHCID 10739106109.7%

Reaction Steps

To a suspension of 1-(tert-butyldiphenylsilyloxymethyl)-2,6-dimethyl-3-nitrobenzene (42 g) and ammonium chloride (4.2 g) in ethanol (378 ml)—water (42 ml) was added iron (7.0 g), and the mixture was refluxed for 6 hours, during which iron (7.0 g) was added thereto twice. Insoluble materials were filtered off, and the filtrate was concentrated. To the residue was added water and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate and concentrated to give 3-amino-1-(tert-butyldiphenylsilyloxymethyl)-2,6-dimethylbenzene (42.8 g) as pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194396B1
Source datasetuspto-grants-2001_02
ORD IDord-795c9415da4e46679d425ad4e0075c3d
Source noteuspto-grants-2001_02