HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851332Generated: October 30, 2026
Ethylene Glycol → 2-(4'-Benzyloxybutyl)-6,6-ethylenedioxy-2-methyloxepane
https://huagongshe.com/reaction/851332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(4'-Benzyloxybutyl)-2-methyl-oxepan-6-one | HCID 13188183 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-(4'-Benzyloxybutyl)-6,6-ethylenedioxy-2-methyloxepane | HCID 13188184 | 99% |
Reaction Steps
p-Toluenesulfonic acid (200 mg) is added to a solution of 2-(4'-benzyloxybutyl)-2-methyl-oxepan-6-one (5.9 g, 0.021 mol), ethylene glycol (30 ml) and dry benzene (200 ml) and the mixture is refluxed for 17 hours in a nitrogen atmosphere with a Dean-Stark apparatus. The solution is cooled and poured into a satd. NaHCO3 solution. The benzene layer is separated and the aqueous phase is extracted with ether (3×50 ml). The organic layers are combined, dried (MgSO4) and the solvents removed at reduced pressure. The crude product is chromatographed on SilicAR CC-7 (125 g) in hexane. Elution with 10% ethyl acetate/hexane gives 2-(4'-benzyloxybutyl)-6,6-ethylenedioxy-2-methyloxepane as a clear colorless oil (6.7 g, 99%): nmr (CDCl3) δ1.10 (s., 3H, CH3), 3.5 (m, 4H, O--CH2 --and O--CH2 --CH2), 3.96 (s, 4H, ketal) 4.48 (s, 2H, O--CH2 --Ph), 730 (s, 5H, aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04384126 |
|---|
| Source dataset | uspto-grants-1983_05 |
|---|
| ORD ID | ord-7cd2bb068ce649d0a97f617100667652 |
|---|
| Source note | uspto-grants-1983_05 |
|---|