HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | HCID 13796806 | HCID 13796806 | — |
| Reactant | HCID 73186994 | HCID 73186994 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | 211.5% |
Reaction Steps
5.2 g of 5-chloro-3-ethyl-2-{(4-methyl-2H-chromen-2-ylidene)methyl}-benzothiazolium p-toluenesulfonate and 4.3 g of 5-chloro-3-ethyl-2-ethylthiobenzothiazolium p-toluenesulfonate were added to 140 ml of acetonitrile and dissolved under heat, and then 4.5 ml of triethylamine was added thereto and reacted for 5 minutes. After cooling the precipitated crystals were separated by filtration and recrystallized from a mixed solvent of methanol/chloroform, to obtain 3.6 g of the desired p-toluenesulfonate product. Yield: 50%. Appearance: Brilliant brown crystal. M.p.: above 240° C. (decomposition). ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04713316 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-90ebf661d4c44964aea67b2bf5a4aba0 |
| Source note | uspto-grants-1987_12 |