HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylene Glycol → HCID 20504189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2,4-Dichlorobenzyl 3-pyridyl ketone | HCID 13671239 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 20504189 | HCID 20504189 | — |
Reaction Steps
2.25 g of 2,4-dichlorobenzyl 3-pyridyl ketone, 2.2 g of p-toluenesulfonic acid monohydrate and 1.0 g of ethylene glycol are heated at reflux for 24 hours in 20 ml of xylene, the resulting water being separated in a water separator. The mixture is then cooled, poured into 2N sodium hydroxide and extracted with diethyl ether, the organic phase is dried over anhydrous sodium sulfate and the solvent is removed under reduced pressure. The crude product is purified by chromatography on silica gel with n-hexane/ethyl acetate (1:1) to yield 3-[2-(2,4-dichlorobenzyl)-1,3-dioxolan-2-yl]pyridine, which melts at 76°-78°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04380544 |
| Source dataset | uspto-grants-1983_04 |
| ORD ID | ord-5cbd657376cf4560bfb2c1a2029f29eb |
| Source note | uspto-grants-1983_04 |