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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604575Generated: October 26, 2026

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

https://huagongshe.com/reaction/1604575

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 numberUS05994368
Source datasetuspto-grants-1999_11
ORD IDord-7fe7b2c75f7f4df8895ded6866753f57
Source noteuspto-grants-1999_11