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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414460Generated: October 25, 2026

Propanoic acid, 2-methyl-3-oxo-, methyl ester → HCID 53839743, compound

https://huagongshe.com/reaction/1414460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropanoic acid, 2-methyl-3-oxo-, methyl esterHCID 103507—
Reactant1-Hexen-3-ol, 4-methyl-HCID 12218386—
ProductHCID 53839743HCID 5383974375.2%

Reaction Steps

57 g (0.5 mole) of 4-methyl-hex-1-en-3-ol and 70 g of α-formylpropionic acid methyl ester (0.6 mole) are heated at from 140° to 200° C whilst stirring; at the same time the methanol liberated is distilled off through a 20 cm column and the carbon dioxide is measured using a gas flow meter. 11.5 liters of carbon dioxide are liberated in the course of three hours. When the elimination of methanol and carbon dioxide has ceased, the mixture is fractionated. 58 g of the above aldehyde (yield: 75% of theory) are obtained. B.p. = 75° - 80° C at 11 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001336
Source datasetuspto-grants-1977_01
ORD IDord-bf6c5d466a1f44208e00480306233c46
Source noteuspto-grants-1977_01