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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165127Generated: November 2, 2026

Dimethyl Sulfate → HCID 14823627, compound

https://huagongshe.com/reaction/2165127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantTetrahydrofuranHCID 8028—
Reactant5-[4-(Methylsulfanyl)phenyl]-2,2'-bithiopheneHCID 23044306—
ReactantButyllithiumHCID 178418339—
CatalystButyllithiumHCID 178418339—
SolventWaterHCID 962—
ProductHCID 14823627HCID 14823627—

Reaction Conditions

Temperature0 °C

Reaction Steps

Under a nitrogen atmosphere, a stirred solution of 0.82 gram (0.003 mole) of 5-(4-methylthiophenyl)[2,2'-bithienyl] in 100 ml of freshly distilled tetrahydrofuran was cooled to 0° C. and 1.4 ml of n-butyllithium (2.6M in hexanes) was added dropwise via syringe during a ten minute period. Upon completion of addition the reaction mixture stirred at 0° C. for 30 minutes, then at ambient temperature for three hours. The reaction mixture was recooled to 0° C. and an additional five drops of n-butyllithium was added. The reaction mixture stirred at 0° C. for one hour then 0.32 ml (0.0034 mole) of dimethylsulfate was added. Upon completion of addition the reaction mixture was stirred at ambient temperature for 16 hours. The reaction mixture was taken up in 70 ml of water and the organic layer was separated. The aqueous layer was washed with three 25 ml portions of chloroform. The organic layers were combined and washed, first with water, then with an aqueous solution saturated with sodium chloride. The organic layer was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to yield 0.78 gram of 5'-methyl-5-(4-methylthiophenyl)[2,2'-bithienyl]; m.p. 145°-147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939165
Source datasetuspto-grants-1990_07
ORD IDord-4685f86124aa489e8b3d68bb4c4988f1
Source noteuspto-grants-1990_07