HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 4-(Benzothiazol-2-ylthio)-butane-1,2,3-tricarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-Butene-1,2,3-tricarboxylic acid | HCID 592363 | — |
| Reactant | HCID 178418395 | HCID 178418395 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(Benzothiazol-2-ylthio)-butane-1,2,3-tricarboxylic acid | HCID 19427569 | — |
Reaction Steps
4.45 g of 2-mercaptobenzthiazole, and 5 g of but-3-ene-1,2,3-tricarboxylic acid are ground with one another in a mortar. The powdered mixture is introduced in portions and with stirring into 60 ml of 70% H2SO4 at 48°-50°, in the course of one hour. After a further 3 hours at 48°-50°, the reaction mixture is cooled to room temperature and diluted with 250 ml of water at 25°-30°, with stirring. The aqueous solution is decanted from a little tacky deposit and is diluted with a further 200 ml of water. After being stirred for 1 hour the precipitate is filtered off and dried. The 4-(benzthiazol-2-ylthio)-butane-1,2,3-tricarboxylic acid obtained melts at 188°-190° after recrystallisation from methanol/water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05152929 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-c914d1a1f2b646759ac84fa4e23072eb |
| Source note | uspto-grants-1992_10 |