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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1283123Generated: November 2, 2026

Ethanol, 2-methoxy-, 1-(4-methylbenzenesulfonate) → HCID 13066475, compound

https://huagongshe.com/reaction/1283123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol, 2-methoxy-, 1-(4-methylbenzenesulfonate)HCID 86977—
ReactantHCID 13066473HCID 13066473—
SolventIsopropanolHCID 3776—
SolventSodiumHCID 5360545—
ProductHCID 13066475HCID 1306647553.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

3 g of 5H-[1]benzopyrano[ 2,3-b]pyridin-7-yl-acetone is dissolved in a solution of 0.32 g of metallic sodium in 15 ml of absolute isopropyl alcohol by warming to 50°-60°C. The solution is cooled to 40°C, 3.5 g of 2-methoxyethyl p-toluenesulfonate is added, and the mixture is stirred under reflux for 1.5 hours. The reaction mixture is concentrated, chloroform and water are added to the residue, and the mixture is stirred. The chloroform layer is separated, dried over anhydrous magnesium sulfate and concentrated. The oily residue is column chromatographed over silica gel (100 g) with a mixture of chloroform and ethyl acetate (10:1) as eluent to give 2.0 g of 3-(5H-[1]benzopyrano[ 2,3-b]pyridin-7-yl)-5-methoxy-2-pentanone as a pale yellow transparent oil. nD28 = 1.5764

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03974168
Source datasetuspto-grants-1976_08
ORD IDord-e3d8e7db89e24e9ab4600ae52246cd7a
Source noteuspto-grants-1976_08