HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126964Generated: October 25, 2026
Benzothiazole → 2-(3-Aminopropylthio)-aniline
https://huagongshe.com/reaction/126964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzothiazole | HCID 7222 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloropropan-1-amine hydrochloride | HCID 145855 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(3-Aminopropylthio)-aniline | HCID 20288563 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254229 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-a8eb211dc1a9495db2f7b22432defe2f |
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| Source note | uspto-grants-1981_03 |
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