HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189404Generated: October 29, 2026
Ethylene Glycol → 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane
https://huagongshe.com/reaction/1189404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | 3'-Bromoacetophenone | HCID 16502 | — |
| Product | 2-(3-Bromophenyl)-2-methyl-1,3-dioxolane | HCID 10999218 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 3′-bromoacetophenone (4.67 mL, 33.89 mmol) in ethylene glycol (36.4 mL) was treated with trimethylorthoformate (7.58 mL, 69.14 mmol) followed by LiBF4 (648 mg, 6.78 mmol). The reaction mixture was heated at 95° C. for 3.5 h. The reaction mixture was cooled to rt and partitioned between ether (100 mL) and sat. aq. Na2CO3 (25 mL). The layers were separated and the aq. layer extracted twice with ether (50 mL). The combined org. extracts were dried over Na2SO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (9:1 hept-EA) gave the title compound as a dark yellow oil. TLC: rf (9:1 hept-EA)=0.44. LC-MS-conditions 02: tR=1.00 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08674111B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-74d6f94912b9441980cb8207ddc13e0f |
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| Source note | uspto-grants-2014_03 |
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