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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700940Generated: October 30, 2026

4,4'-Dichlorodiphenylmethane → 1,1'-(4-Chlorobutane-1,1-diyl)bis(4-chlorobenzene)

https://huagongshe.com/reaction/1700940

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4'-DichlorodiphenylmethaneHCID 7576—
Reactant1-Chloro-3-iodopropaneHCID 81363—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1,1'-(4-Chlorobutane-1,1-diyl)bis(4-chlorobenzene)HCID 1831904144%

Reaction Steps

A solution of 4,4′-dichlorodiphenylmethane (4.37 g, 18.4 mmol) (Blackwell, J. et all, J. Chem. Soc., 1961, 1405) in dry tetrahydrofuran (50 ml) was treated at 0° C. with butyllithium (12.1 ml of 1.6 M, 19.36 mmol) added dropwise over 15 min. After 15 min, the red solution was then added dropwise to a cold (−78° C.) solution of 1-chloro-3-iodopropane (15.0 g, 73.4 mmol) in dry tetrahydrofuran (120 ml). After 20 min at −78° C., the reaction mixture was quenched by the addition of saturated ammonium chloride (100 ml) and diluted with toluene. The organic phase was washed with brine and dried. The oil obtained after evaporation of the solvent was purified on silica gel (elution hexane-toluene 85:15) and distilled under vacuum to give 2.54 g (44%) of the title material as a clear oil: bp 110-130° C./1.5 torr (air bath temperature).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350892B1
Source datasetuspto-grants-2002_02
ORD IDord-4906f058dea0494c8e6b83d9991829bf
Source noteuspto-grants-2002_02