HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757581Generated: October 28, 2026
p-Toluenesulfonic acid → HCID 15292071, compound
https://huagongshe.com/reaction/1757581
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | HCID 54380635 | HCID 54380635 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15292071 | HCID 15292071 | — |
Reaction Steps
Phenylacetyl chloride (0.6 mL, 4.5 mmole) was added to a solution of 5,6-dimethyl-N4 -(2-phenylethyl)-N2,N2 -bis(phenylmethyl)pyridine-2,3,4-triamine (1 96 g, 4.5 mmole) in methylenechloride (100 mL) and the resulting mixture was stirred at ambient temperature overnight. A catalytic amount of p-toluenesulfonic acid was added and stirring was continued at ambient temperature over the weekend. The reaction mixture was washed with saturated sodium bicarbonate solution, dried over magnesium sulfate then concentrated under vacuum to provide an oil. The oil was purified by silica gel column chromatography eluting with 5-10% ethyl acetate in hexane to provide 1.8 g of the desiredproduct as a white solid, m.p. 139°14 141° C. Analysis: Calculated for C37H36N4 : % C, 82.80; % H, 6.76; % N, 10.44; Found: % C, 82.86; % H, 6.78; % N, 10.36.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05446153 |
|---|
| Source dataset | uspto-grants-1995_08 |
|---|
| ORD ID | ord-3f26414b656a424fb932084c299711a4 |
|---|
| Source note | uspto-grants-1995_08 |
|---|