HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 265298Generated: October 30, 2026
2-Benzyl-1,3-dioxolane → HCID 19082234, compound
https://huagongshe.com/reaction/265298
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Benzyl-1,3-dioxolane | HCID 7562 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Bromopropionitrile | HCID 17020 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19082234 | HCID 19082234 | 90% |
Reaction Steps
A mixture of 3-(2-phenylethoxy)ethanol (8.0 g, prepared from 2-phenylmethyl 1,3-dioxolane according to the general method in Can. J. Chem., 1974, 52, 888), 3-bromopropanenitrile (5.6 ml), sodium hydroxide (50 g) and tetrabutylammonium chloride (0.5 g) in dichloromethane (100 ml) and water (100 ml) was stirred at room temperature for 72 hours. The mixture was diluted with water and the organic layer separated. The aqueous layer was extracted with a further portion of dichloromethane. The combined organic extracts were washed with dilute aqueous hydrochloric acid and water, dried (MgSO4) and evaporated under reduced pressure to yield the crude product. This material was purified by flash chromatography over silica using 1:1 ether:petroleum ether (bp 60°-80°) as eluant to give the subtitled compound as an oil (9.84 g, 90% ).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05648370 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-00d7d368ac524d61bd2219f2643035b6 |
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| Source note | uspto-grants-1997_07 |
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