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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625768Generated: November 2, 2026

Triethylsilane → 3-Bromo-(5-ethyl-2-thienylmethyl)benzene

https://huagongshe.com/reaction/1625768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromophenyl-5-ethyl-2-thienylmethanolHCID 61100862—
SolventDichloromethaneHCID 6344—
Product3-Bromo-(5-ethyl-2-thienylmethyl)benzeneHCID 4693043093.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

The above 3-bromophenyl-5-ethyl-2-thienylmethanol (2.90 g) was dissolved in dichloromethane (38 ml), and the mixture was cooled to −78° C. under argon atmosphere. To the mixture were added triethylsilane (6.18 ml) and boron trifluoride diethyl ether complex (2.45 ml), and the mixture was gradually warmed to room temperature over a period of one hour. The mixture was basified with a saturated aqueous sodium hydrogen carbonate solution, and the dichloromethane layer was collected, dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane) to give the desired 3-bromo-(5-ethyl-2-thienylmethyl)benzene (2.57 g) as a colorless syrup. APCI-Mass m/Z 281/283 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-454deec6463c4a85bb1ea1c4960b92fb
Source noteuspto-grants-2014_07