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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646791Generated: October 31, 2026

Ethanol → HCID 15230859, compound

https://huagongshe.com/reaction/1646791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14651334HCID 14651334—
ProductHCID 15230859HCID 1523085984%

Reaction Steps

4-Phenyl-4-(3,5,6-trimethyl-1,4-benzoquinon -2-yl)butanoic acid (1.2 g) was dissolved in ethanol (50 ml), and thionyl chloride (0.4 ml) was added to the solution, followed by stirring at room temperature for 4 hours. After the reaction solution was concentrated under reduced pressure, the resulting residue was dissolved in isopropyl ether, and the organic layer was washed with water, dried and concentrated under reduced pressure. The residue was chromatographed on a silica gel column, and the object compound was eluted with isopropyl ether to give ethyl 4-phenyl-4-(3,5,6-trimethyl-1,4-benzoquinon -2-yl)butanoate (1.1 g, 84%). Its typical physical properties and nuclear magnetic resonance spectrum data are shown in Table 1. By following the procedure of this example, the Compound No. 42 was prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180742
Source datasetuspto-grants-1993_01
ORD IDord-7229d093559b4f6eb1589415befe3083
Source noteuspto-grants-1993_01