HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267539Generated: October 30, 2026
Ethylene Glycol → 2-Hydroxyethyl 2-Bromopropionate
https://huagongshe.com/reaction/1267539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Bromopropanoyl chloride | HCID 97980 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Hydroxyethyl 2-Bromopropionate | HCID 11041698 | 56% |
Reaction Steps
In a nitrogen atmosphere, 2-bromopropionyl chloride (2 mL, 3.35 g, 19.5 mmol) was slowly added dropwise at 0° C. to a THF solution (10 mL) containing ethylene glycol (10.9 mL, 195 mmol) and pyridine (3 g, 39 mmol). The resulting solution was stirred at the same temperature for 2 hours. Dilute hydrochloric acid and ethyl acetate were added and mixture was allowed to separate into two phases. The organic phase was washed with dilute hydrochloric acid and brine, and dried over Na2SO4. The volatile matter was distilled off under reduced pressure and a crude product (3.07 g) was obtained. This crude product was distilled under reduced pressure (70-73° C., 0.5 mm Hg) to give hydroxyethyl 2-bromopropionate (2.14 g, 56%) represented by the following formula:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552118B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-b6f30ad298c743158692b94720ce8fa2 |
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| Source note | uspto-grants-2003_04 |
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