HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → p-[(1,5-Dimethylhexyl)oxy]benzoic acid propargyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | HCID 54404637 | HCID 54404637 | — |
| Product | p-[(1,5-Dimethylhexyl)oxy]benzoic acid propargyl ester | HCID 53978508 | — |
Reaction Steps
13 g of p-[(1,5-dimethylhexyl)oxy]benzoic acid methyl ester is heated to reflux with 9 g of propargyl alcohol and 0.1 g of p-toluenesulphonic acid. The excess propargyl alcohol is thereupon slowly (5 hrs.) distilled off. The residue is poured onto water and extracted with diethyl ether. The ether phase is dried with sodium sulfate and evaporated. There is obtained dark-yellow p-[(1,5-dimethylhexyl)oxy]benzoic acid propargyl ester which is purified on Kieselgel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138579 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-7e44eb09f9e54fe7ab797be45c72927f |
| Source note | uspto-grants-1979_02 |