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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006074Generated: October 31, 2026

Ammonium Chloride → Bis(2-methyl-4-thienyl)methane

https://huagongshe.com/reaction/1006074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-2-methylthiopheneHCID 638584—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant5-Methylthiophene-3-carbaldehydeHCID 6502011—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductBis(2-methyl-4-thienyl)methaneHCID 22639087—

Reaction Conditions

Temperature-65 °C

Reaction Steps

31.3 g of 2-methyl-4-bromo-thiophene (0.177 mol) was dissolved in 150 ml ether and treated dropwise with 113 ml 1.6M BuLi (0.18 mol) at −70° C. The resulting solution kept under stirring at −60 to −70° C. for 30 min and then was treated with 22.3 g 2-methyl-4-thiophene-aldehyd (0.177 mol) in 100 ml ether. The mixture was allowed to warm to r.t., then neutralized by 10% aq. NH4Cl and washed with water. The organic phase was collected and evaporated off. The suspension of 10 g LiAlH4 (0.266 mol) in 100 ml ether was treated dropwise with the solution of 35.5 g AlCl3 (0.266 mol) in 100 ml ether. The resulting mixture was treated with the solution of the compound obtained in the previous reaction in 100 ml ether. The mixture refluxed for additional 1 h, cooled up to r.t. and treated with 100 ml ethyl acetic ester. Then the mixture was treated with 300 ml H2O and 300 ml ether. Organic phase was collected, washed with water, dried over MgSO4 and evaporated off. The residue was distilled at 90-110/0.5 mmHg. Yield 23.2 g (63%). The title compound was analyzed by 1H-NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787619B2
Source datasetuspto-grants-2004_09
ORD IDord-aaf5031c8be14b32947fb64fe8b4f1f2
Source noteuspto-grants-2004_09