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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259919Generated: October 25, 2026

Tetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonate → Tetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonate

https://huagongshe.com/reaction/259919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonateHCID 22917835—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonateHCID 9803422—

Reaction Conditions

Temperature25 °C

Reaction Steps

0.2 g of 5% strength palladium on charcoal is added to a solution of 2.8 g of the laevorotatory isomer of tetra-n-butylammonium 1-(3-nitrophenyl)ethanesulphonate in 50 cm3 of ethanol. The suspension is stirred for 2 hours at a temperature of about 25° C. under a hydrogen atmosphere (100 kPa). The catalyst is filtered off and the filtrate is concentrated to dryness under reduced pressure (2.7 kPa) at 40° C. 2.8 g of the laevorotatory isomer of tetra-n-butylammonium 1-(3-aminophenyl)ethanesulphonate are thus obtained in the form of an oil, used as such in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05523469
Source datasetuspto-grants-1996_06
ORD IDord-e4772676ca694072bc9fb6329cecc7d7
Source noteuspto-grants-1996_06