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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974374Generated: October 27, 2026

2-Nitropropane → 3-Bromo-7-benzothiophene-carbaldehyde

https://huagongshe.com/reaction/974374

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NitropropaneHCID 398—
ReactantSodiumHCID 5360545—
Reactant3-Bromo-7-bromomethylbenzothiopheneHCID 14780522—
SolventEthanolHCID 702—
Product3-Bromo-7-benzothiophene-carbaldehydeHCID 19986344—

Reaction Steps

With stirring, 68.2 g (0.74 mole) of 2-nitropropane are added dropwise at room temperature, over a period of 45 minutes, to a Na-ethoxide solution prepared under an argon atmosphere from 14.2 g (0.61 mole) of sodium and 800 ml of abs. ethanol. 137 g (0.61 mole) of 3-bromo-7-bromomethylbenzothiophene are then added dropwise at room temperature, over a period of 1.5 hours, to the resulting white suspension. After the reaction mixture has been stirred for one day, the solvent is evaporated off from the reaction mixture in vacuo, the resulting residue of 101.2 g is dissolved in a mixture of hexane:diethyl ether 1:1 and the solution is purified by chromatography on silica gel. After evaporation of the solvent, 81 g (80% of the theoretical amount) of 3-bromo-7-benzothiophene-carbaldehyde are obtained as residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05068359
Source datasetuspto-grants-1991_11
ORD IDord-1ae22274ec364f248ee7d34599f174ce
Source noteuspto-grants-1991_11