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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6192Generated: October 26, 2026

3-Mercaptopropionic Acid → N-(4-Anilinophenyl)-3-sulfanylpropanamide

https://huagongshe.com/reaction/6192

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Mercaptopropionic AcidHCID 6514—
ReactantO-XyleneHCID 7237—
ReactantN-Phenyl-p-phenylenediamineHCID 7564—
SolventHexaneHCID 8058—
ProductN-(4-Anilinophenyl)-3-sulfanylpropanamideHCID 19795022—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 18.4 grams of N-phenyl-p-phenylene diamine, 10.6 grams of β-mercaptopropionic acid and 120 milliliters of xylene (technical grade) was heated to reflux (about 140° C.) under nitrogen atmosphere, with stirring. A 1.6 milliliter quantity of water (90% of theory) was removed from this mixture by azetropic distillation through a Vigreux column with the aid of Dean-Start trap, during a 13-hour period. A solid product was isolated in 18.7 grams quantity from the reaction mixture by cooling the latter, pouring into hexane, collecting the resultant crystalline product by filtration, washing the crushed crystalline product with more hexane and evaporating to dryness. The product was recrystallized from hot toluene to 17.6 grams (64.5%) of white platelets melting at 98.3°-99.5° C. The resultant new compound, N-(4-anilino-phenyl)beta-mercaptopropionamide, sometimes referred to hereafter as MPDA, had mercaptan assay of 93.8% of theoretical, on the basis of a potentiometric titration with an isopropyl alcohol solution of silver nitrate, following a method described R. M. Pierson, A. J. Costanza and A. H. Weinstein, J. Polymer Sci., 17, 234 (1955).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05247027
Source datasetuspto-grants-1993_09
ORD IDord-b17abff2b44840dd9b7ca02149e953e2
Source noteuspto-grants-1993_09