HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → HCID 21481848, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Acetal | HCID 7765 | — |
| Reactant | HCID 561596 | HCID 561596 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21481848 | HCID 21481848 | — |
Reaction Steps
3-Benzyloxy-2-methylpropane-1,2-diol (5.0g), 1,1-diethoxyethane (3.0g) and p-toluenesulphonic acid were heated at 110°-115° C with stirring until no more alcohol was evolved. The mixture was then heated at 140°-145° C for 15 minutes. After cooling, the mixture was dissolved in ether and the resulting solution was then washed with 5% potassium carbonate solution followed by water. The solution was dried over anhydrous magnesium sulphate and the solvent was removed under reduced pressure to yield a liquid which on distillation gave the desired product having a b.p. 81°-82° C at 0.3 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04004911 |
| Source dataset | uspto-grants-1977_01 |
| ORD ID | ord-940f615aa68d4e07aff405dfd494fde3 |
| Source note | uspto-grants-1977_01 |