HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 21569624, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-phenacyl-1-tetralone | HCID 12270346 | — |
| Reactant | HCID 21569607 | HCID 21569607 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21569624 | HCID 21569624 | — |
Reaction Steps
A mixture of 2.6 g. (0.01 mole) of 2-phenacyl-1-tetralone, 2.3 g. (0.01 mole) of dimethylphosphinylmethyl p-aminobenzoate, 0.4 g. of p-toluenesulfonic acid, and 250 ml. of dry toluene was heated under reflux for 73 hours, concentrated to about 100 ml., diluted with 25 ml. of cyclohexane, and cooled. The solid which separated was collected to provide 2.6 g. (57%) of solid, m.p. 171°-173°. Recrystallization from cyclohexane-benzene gave pale yellow crystals, m.p. 180°-181°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931407 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-62502f782efd4959b2f2966e1003eaec |
| Source note | uspto-grants-1976_01 |