HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488580Generated: October 29, 2026
Ethylene Glycol → 2-methyl-1,3-dioxolane-2-carboxylic acid
https://huagongshe.com/reaction/488580
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Ethyl pyruvate | HCID 12041 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-methyl-1,3-dioxolane-2-carboxylic acid | HCID 298859 | 38% |
Reaction Steps
To a stirred mixture containing ethyl pyruvate (11.1 mL, 0.1 mol) and ethylene glycol (5.6 mL, 0.1 mol) in anhydrous dichloromethane (100 mL) at 0° C. was added boron trifluoride dietherate (6.4 mL, 0.05 mol) and catalytic amount of acetic acid. The resulting mixture was stirred at 40° C. for 16 h and then diluted with 100 mL of dichloromethane. The organic solution was washed successively with saturated sodium chloride solution (2×80 mL). The organic layer was separated and the combined organic extracts were concentrated. The residue was treated with 1N sodium hydroxide at room temperature. After stirring at room temperature for 3 h (monitored by TLC), citric acid was added to adjust the pH to 4. The product was extracted with dichloromethane, dried over Na2SO4 and concentrated to afford 5.1 g (38%) of the title compound (129) as a clear liquid. This material was used in the next reaction without further purification. 1H NMR (CDCl3, 400 MHz): δ 1.55 (s, 3H), 4.03 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06972341B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-c0dad070a58347ec971c99ffffb428b2 |
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| Source note | uspto-grants-2005_12 |
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