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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126964Generated: October 25, 2026

Benzothiazole → 2-(3-Aminopropylthio)-aniline

https://huagongshe.com/reaction/126964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzothiazoleHCID 7222—
ReactantSodium HydroxideHCID 14798—
Reactant2-Chloropropan-1-amine hydrochlorideHCID 145855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-(3-Aminopropylthio)-anilineHCID 20288563—

Reaction Conditions

Temperature70 °C

Reaction Steps

270 parts of benzothiazole and 160 parts of sodium hydroxide are boiled under reflux for 3 hours in 400 parts of water. After cooling to 70° C., 250 parts of methanol are added, followed by the dropwise addition over a period of 2 hours at 70° C. of a solution of 260 parts of 2-chloropropylamine·HCl in 500 parts of water. After stirring for another 3 hours at 100° C., the mixture is cooled and a solution of 100 parts of sodium hydroxide in 200 parts of water is added to it. The organic phase is separated off, the aqueous phase is washed twice with 200 parts of toluene and the combined organic phases are concentrated by evaporation, leaving 346 parts of 2-(3-aminopropylthio)-aniline in the form of a yellowish liquid boiling at 130° C./0.04 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04254229
Source datasetuspto-grants-1981_03
ORD IDord-a8eb211dc1a9495db2f7b22432defe2f
Source noteuspto-grants-1981_03