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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075629Generated: November 1, 2026

Water → 1-Phenyl-2,5,8,11,14-pentaoxahexadecan-16-ol

https://huagongshe.com/reaction/2075629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium HydroxideHCID 14797—
ReactantPentaethylene glycolHCID 62551—
SolventDichloromethaneHCID 6344—
Product1-Phenyl-2,5,8,11,14-pentaoxahexadecan-16-olHCID 1355369232.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

To Compound 1 (5.2 g, 21.8 mmol), potassium hydroxide (1.2 g, 21.4 mmol) was added; this was followed by stirring on an oil bath at 130° C. for 15 minutes, after which the oil bath was removed and benzyl chloride (2.7 g, 21.3 mmol) was gradually added. This was again heated to 130° C. and stirred for 2 hours. After the solution was allowed to cool to room temperature, water was poured to stop the reaction, and extraction from methylene chloride was conducted. The combined organic phases were dried with sodium sulfate, filtered, and concentrated under reduced pressure, after which the residue obtained was purified by silica gel column chromatography (Yamazen YFLC Gel, eluent (ethyl acetate—5% methanol-ethyl acetate solution) to yield Compound 19 (light-yellow oil 2.3 g, 32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919653B2
Source datasetuspto-grants-2011_04
ORD IDord-c7dbf4724894463f8b7944dbcde27db6
Source noteuspto-grants-2011_04