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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252261Generated: November 1, 2026

2-Bromo-3-methylthiophene → HCID 10241021, compound

https://huagongshe.com/reaction/252261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-3-methylthiopheneHCID 84314—
Reactant2-Methylpropyl 4-methylbenzene-1-sulfonateHCID 310590—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
ProductHCID 10241021HCID 1024102148%

Reaction Steps

A part of a solution containing 2-bromo-3-methylthiophene (1.5 g, 8.5 mmol) in dry diethyl ether is added drop-wise to a suspension of magnesium (308 mg, 12.7 mmol, 1.5 equiv.) in dry diethyl ether until the mixture starts to reflux. The remaining solution is added dropwise. A solution of toluene-4-sulfonic acid isobutyl ester (2.9 g, 12.7 mmol, 1.5 equiv.) in dry diethyl ether is added dropwise at room temp., then the mixture is further refluxed for two hours. After cooling to room temp., the mixture is quenched with sat. ammonium chloride solution and extracted with tert. butylmethylether. The combined organic extracts are washed with water, brine, dried over magnesiumsulfat-dihydrate, filtered and evaporated to give a yellow oil. After Kugelrohr-distillation, 630 mg of the title compound is obtained as a colorless oil. GC-MS (EI): M=154

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868030B2
Source datasetuspto-grants-2011_01
ORD IDord-d9295be04517405aa91c4ff1746a84e0
Source noteuspto-grants-2011_01