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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483071Generated: October 25, 2026

1-Bromopentane → 2-n-Pentoxy-5-nonyl benzophenone

https://huagongshe.com/reaction/483071

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantSodium HydroxideHCID 14798—
ReactantMethanone, (2-hydroxy-5-nonylphenyl)phenyl-HCID 93939—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-n-Pentoxy-5-nonyl benzophenoneHCID 5389387382%

Reaction Steps

A solution of 2-hydroxy-5-nonyl benzophenone, 15 g, in 100 mL methylene chloride was mixed with a solution of 9.25 g NaOH in 100 mL water. To this mixture was added 6.9 g n-pentyl bromide and 1.48 g tetra-n-butylammonium bromide. The whole mixture was then vigorously agitated overnight at 40° C. After cooling to room temperature with 50 mL CH2Cl2. The combined methylene chloride layers were concentrated to an oil, which was taken up in 100 mL petroleum ether and washed with 100 mL water. Finally, the organic layer was dried over anhydrous magnesium sulfate and the volatiles removed under vacuum to give 15 g (82% yield) of 2-n-pentoxy-5-nonyl benzophenone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578250
Source datasetuspto-grants-1986_03
ORD IDord-c311d96f2e954f6182650344fbe57b25
Source noteuspto-grants-1986_03