HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → p-Toluenesulfonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 20442582 | HCID 20442582 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | p-Toluenesulfonic acid | HCID 6101 | 164% |
Reaction Steps
1-(2-Acetylthioethyl)-5-triphenylmethylaminomethyltetrazole, (e) (300 mg) in acetone (3 ml) was cooled to -20° and treated with p-toluenesulphonic acid monohydrate (128 mg) in acetone (2 ml). The reaction mixture was allowed to warm to room temperature and stirred for 7 hours. The resultant colourless solid was filtered off to give the p-toluenesulphonic acid salt (f) (190 mg), m.p. 184°-185°, νmax (KBr)1680, 1235, 1225, 1170, 1150, 1130, 1042, 1015, 838, 688, 572 cm-1, (D2O) 2.28 (3H,s), 2.35 (3H,s), 3.34 (2H, t, J Ca 6 Hz), 7.30 (2H, d, J 9 Hz), 7.65 (2H, d, J 9 Hz)ppm. Other signals were obscured by the HOD signal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04477662 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-096d7aed045a4dfa8b13684490d2a1ce |
| Source note | uspto-grants-1984_10 |