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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21525Generated: October 30, 2026

Benzyl Alcohol → Benzyl {o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetate

https://huagongshe.com/reaction/21525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant{o-[5-(2,4-Dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetyl chlorideHCID 19932413—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl {o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetateHCID 5416848177.8%

Reaction Steps

Benzyl alcohol (0.8 mL, 7.73 mmol) and triethylamine (1 mL, 7.17 mmol) are added to a mixture of {o-[5-(2,4-dichlorophenoxy)-2-nitrophenoxy]phenoxy}acetyl chloride (1.12 g, 2.38 mmol) in tetrahydrofuran. The reaction mixture is stirred for twenty minutes, poured into water and extracted with ether. The combined organic extracts are washed sequentially with one molar hydrochloric acid, water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain an oil. Column chromatography of the oil using silica gel and a hexanes in methylene chloride solution gives the title product as a yellow oil (1.0 g) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424280
Source datasetuspto-grants-1995_06
ORD IDord-747da01c1a934f2ca7eb9695b5039c16
Source noteuspto-grants-1995_06