HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → HCID 86739786, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Toluenesulfonate | HCID 85570 | — |
| Reactant | HCID 10379527 | HCID 10379527 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86739786 | HCID 86739786 | — |
Reaction Steps
The alcohol is converted to the tosylate by dissolving in methylene chloride containing N,N-dimethyl-4-aminopyridine (0.05 mol eq) and triethylamine (1.05 mol eq) and treating with tosyl chloride (1.1 mole eq) added in one portion at 0° C. with stirring. After standing for about 24 hr. at 0° C., the mixture is treated with water and extracted several times with methylene chloride. The combined methylene chloride extracts are dried over magnesium sulfate, filtered and concentrated under reduced pressure. Flash chromatography of residual material affords 2-[3-(p-toluenesulfonate)propyl]-5-ethyl-2,4-dihydro-4-(2-phenoxyethyl)-3H-1,2,4-triazol-3-one (XV, Y=H, X1 =0, n=2, R2 =C2H5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04487773 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-ca12cd3df928430db815c350cc4a9720 |
| Source note | uspto-grants-1984_12 |