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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59752Generated: October 25, 2026

Ammonium Chloride → 3-Bromo-5-(diethoxymethyl)-2-nitrothiophene

https://huagongshe.com/reaction/59752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl orthoformateHCID 31214—
Reactant4-Bromo-5-nitrothiophene-2-carbaldehydeHCID 21886281—
SolventEthanolHCID 702—
Product3-Bromo-5-(diethoxymethyl)-2-nitrothiopheneHCID 8670385881.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 4-bromo-5-nitrothiophene-2-carbaldehyde (Int. 65) (6.981 g, 29.6 mmol) in EtOH (50 ml), ammonium chloride (0.475 g, 8.87 mmol) and triethyl orthoformate (7.39 ml, 44.4 mmol) were added, and the resulting solution was stirred at 60° C. for 14 hours. Additional triethyl orthoformate (7.39 ml, 44.4 mmol) was added, and the mixture was vigorously refluxed for further 2 days. The solvent was evaporated under vacuum and the crude was partitioned between water and EtOAc. The organic phase was washed with brine, dried over sodium sulfate, filtered and evaporated. The crude was purified by chromatography on silica gel cartridge (petroleum ether/EtOAc=9/1) to afford 3-bromo-5-(diethoxymethyl)-2-nitrothiophene (Int. 66) (7.456 g, 24.04 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440954B2
Source datasetuspto-grants-2016_09
ORD IDord-4d4f5ea7519745e492b3a0bb2f41119c
Source noteuspto-grants-2016_09