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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296848Generated: October 30, 2026

4-Chloro-1-naphthol → 2-Chloro-1-(4-((4-chloronaphthyloxy)methyl)phenoxy)ethane

https://huagongshe.com/reaction/1296848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-1-naphtholHCID 11787—
ReactantTributylphosphineHCID 13831—
Reactant[4-(2-Chloroethoxy)phenyl]methanolHCID 21882321—
Reactant(4-(2-Bromoethoxy)phenyl)methanolHCID 22482237—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-1-(4-((4-chloronaphthyloxy)methyl)phenoxy)ethaneHCID 23514395—

Reaction Steps

A stirred solution of 8.4 grams (0.045 mole) of the mixture of (4-(2-bromoethoxy)phenyl)methan-1-ol and (4-(2-chloroethoxy)phenyl)methan-1-ol, 8.1 grams (0.045 mole) of 4-chloronaphthol, and 13.7 mL (0.054 mole) of tributylphosphine in 500 mL of THF was cooled in an ice bath and 12.6 grams (0.049 mole) of 1-1′-(azodicarbomyl)dipiperidine was added. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it stirred for 24 hours. After this time, the solvent was reduced under reduce pressure, yielding a solid. The solid was purified by column chromatography on silica gel, yielding 15 grams of crude product. The crude product was further purified by column chromatography on silca gel, yielding 6.7 grams of title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247756B2
Source datasetuspto-grants-2007_07
ORD IDord-82d21bd388de45c68246bab1be70f9be
Source noteuspto-grants-2007_07