HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965407Generated: October 30, 2026
4-Toluenesulfonyl chloride → HCID 86752876, compound
https://huagongshe.com/reaction/965407
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Hydroxyacetamidine | HCID 30926 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86752876 | HCID 86752876 | 130.5% |
Reaction Steps
Triethylamine (3 ml, 2.18 g, 0.022 mol) was added to acetamide oxime (1.5 g, 0.02 mol) in tetrahydrofuran (THF) (45 ml). To the mixture, p-toluenesulfonyl chloride (Tosylchloride, TsCl) (4.2 g, 0.022 mol) was added in small portions (generating heat intensively). The mixture was allowed to react at room temperature for 45 mins. and the precipitates were collected by filtration. THF was distilled off under reduced pressure, and water was added to the resultant residue. The residue was extracted with ethyl acetate, and the organic layer was washed with water and dried over sodium sulfate. The ethyl acetate was distilled off under reduced pressure, and isopropyl ether was added to the residue to separate crystals. The crystals were filtered off is and dried to give acetamide-oxime-tosylate (3.2 g, yield; 69.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05773624 |
|---|
| Source dataset | uspto-grants-1998_06 |
|---|
| ORD ID | ord-6681cfa0b13947e59caa2063f893b74c |
|---|
| Source note | uspto-grants-1998_06 |
|---|