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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247227Generated: October 24, 2026

Water → 2-Methoxy-5-nonyl benzophenone

https://huagongshe.com/en/reaction/247227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantMethanone, (2-hydroxy-5-nonylphenyl)phenyl-HCID 93939—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
Product2-Methoxy-5-nonyl benzophenoneHCID 2016199185%

Reaction Steps

A sample of 2-hydroxy-5-nonyl benzophenone (25 g, 0.077 mol) was dissolved in 100 mL methylene chloride. To this solution was added a solution of 20 g (0.5 mol) sodium hydroxide in 100 mL deionized water, followed by the addition of 22 g (0.154 mol) iodomethane and 2.5 g (0.006 mol) tetra-n-butylammonium bromide. The entire mixture was agitated with vigorous mechanical stirring for 1.5 hours at 45° C. The reaction mixture was allowed to cool, and the layers separated. The aqueous phase was extracted with 50 mL methylene chloride. The combined organic layers were dried over anhydrous magnesium sulfate and concentrated under vacuum. The residual oil was taken up in petroleum ether, washed with water, dried over magnesium sulfate and again concentrated under vacuum to provide 22 g (85% yield) of 2-methoxy-5-nonyl benzophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04705896
Source datasetuspto-grants-1987_11
ORD IDord-02cf0dcdccc24239a71a435376af0989
Source noteuspto-grants-1987_11