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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168071Generated: October 28, 2026

Methyl 3-oxovalerate → methyl (E)-3-methoxy-2-pentenoate

https://huagongshe.com/reaction/1168071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-oxovalerateHCID 121699—
ReactantMethylorthoformateHCID 53629101—
ReactantHCID 178418416HCID 178418416—
Productmethyl (E)-3-methoxy-2-pentenoateHCID 5527349—

Reaction Steps

A 250-ml 2-necked round-bottomed flask was equipped with a magnetic stirring bar, a thermometer and an argon inlet. To a mixture of 30.00 g of methyl 3-oxovalerate (0.225 mol) and 125 ml of methyl orthoformate (121.1 g, 1.12 mol) was added under stirring 7.5 g of amberlist 15. The reaction was slightly exothermal at beginning and the temperature reached 31° C. A check with Drager test tube indicated the development of carbon monoxide. The suspension was stirred at rt for 3 h and then filtered into a 500-ml 4-necked pear-shaped flask equipped with an oil bath, a thermometer, an argon inlet, a 20-cm Vigreux column with a distillation head, a vacuum pump with vacuum controller and a cold trap. The volatile components of the reaction mixture were removed by distillation at a still temperature between 37 and 48° C. and a pressure between 250 and 40 mbar. The head temperature reached max 30° C. The residue, 31.3 g Methyl (E)-3-methoxy-2-pentenoate as a yellow oil was used without purification in the next step (theor. amount 32.5 g calculated as enol ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620941B2
Source datasetuspto-grants-2003_09
ORD IDord-f0b7aad059e540eb95ed3c7c00851db7
Source noteuspto-grants-2003_09