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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418178Generated: October 31, 2026

Acetic Acid → 2-t-Butyl-5-(t-butyldimethylsilyloxymethyl)aniline

https://huagongshe.com/reaction/1418178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2-t-Butyl-5-(t-butyldimethylsilyloxymethyl)-1-nitrobenzeneHCID 19348448—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
Product2-t-Butyl-5-(t-butyldimethylsilyloxymethyl)anilineHCID 19348703—

Reaction Steps

81 g (1.24 mol) of zinc powder were added to a solution of 25.19 g (77.9 mmol) of 2-t-butyl-5-(t-butyldimethylsilyloxymethyl)-1-nitrobenzene (prepared as described in Preparation 11) in 270 ml of methanol, and then 10.8 ml of acetic acid were added to the resulting mixture, with ice-cooling. After the exothermic reaction had subsided, the reaction mixture was heated under reflux for 3 hours and then allowed to cool to room temperature, after which it was filtered using a Celite (trade mark) filter aid, and the zinc used was washed with methanol. The filtrate was combined with the washings and the combined mixture was concentrated by evaporation under reduced pressure. The concentrate was dissolved in ethyl acetate, and the resulting solution was washed with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure, to give 22.9 g (a quantitative yield) of the title compound as an oily substance. The compound could be used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880147
Source datasetuspto-grants-1999_03
ORD IDord-8270928d231542a093d420e45be23bb6
Source noteuspto-grants-1999_03