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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374228Generated: November 1, 2026

Acetic Acid → methyl 3-cyclopropyl-2,3-epoxypropionate

https://huagongshe.com/reaction/1374228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl chloroacetateHCID 7295—
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Productmethyl 3-cyclopropyl-2,3-epoxypropionateHCID 1130956770%

Reaction Conditions

Temperature-10 °C

Reaction Steps

A 300-ml three-necked flask equipped with a thermometer and a stirrer was charged with 87 g (0.45 mole) of a 28% sodium methoxide solution in methanol and 21 g (0.30 mole) of cyclopropanecarbaldehyde and, after the contents had been cooled down to −10° C., 48.9 g (0.45 mole) of methyl chloroacetate was added dropwise over 3 hours. After completion of the addition, the reaction mixture was allowed to be warmed up to room temperature and was then stirred at room temperature for 5 hours. Thereafter, 12 g (0.20 mole) of acetic acid was added to neutralize remaining sodium methoxide and the resulting mixture was poured into 140 g of water. The reaction mixture thus obtained was extracted three times each with 50 ml of ethyl acetate and the extracts were washed with 50 ml of saturated salt water. The mixture thus washed was dried over anhydrous sodium sulfate and condensed. The residue was distilled under reduced pressure to yield, as distillates at 70 to 73° C. [6 mmHg (8.0 hPa)], 29.8 g (0.21 mole; yield: 70.0%) of methyl 3-cyclopropyl-2,3-epoxypropionate having the following properties.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07164047B2
Source datasetuspto-grants-2007_01
ORD IDord-6ffdc331deb04eb49930410b3019191e
Source noteuspto-grants-2007_01