HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697623Generated: October 31, 2026
2-Chloroethanol → 2-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid Ethyl Ester
https://huagongshe.com/reaction/1697623
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 2-(4-bromophenyl)-2-oxoacetate | HCID 10729811 | — |
| Reactant | Potassium tert-butoxide | HCID 86639980 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromo-phenyl)-[1,3]dioxolane-2-carboxylic Acid Ethyl Ester | HCID 66772046 | 58% |
Reaction Steps
To a solution of ethyl-4-bromobenzoylformate (940 mg) and 2-chloroethanol (0.360 mL) in a 2:1 mixture of dimethylformamide:tetrahydrofuran (2.1 mL) was added dropwise at −60° C. a solution of potassium tert-butanol (0.597 mg) in dimethylformamide (2 mL). The reaction mixture was stirred at −60° C. for 4 h then allowed to warm up to room temperature and stirred at room temperature overnight. The reaction mixture was partitioned between an aqueous solution of ammonium chloride and ethyl acetate. The aqueous layer was extracted with ethyl acetate and the combined organic layer were washed with brine. The crude mixture was concentrated to dryness and purified by chromatography on silica gel to yield the title compound as a colorless liquid (616 mg; 58%). MS (ESI): m/z=300.8 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163793B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-7fb622fe119b449c9486b2338dee5d13 |
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| Source note | uspto-grants-2012_04 |
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