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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59753Generated: October 26, 2026

Methanol → 5-(Diethoxymethyl)-3-methoxy-2-nitrothiophene

https://huagongshe.com/reaction/59753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Bromo-5-(diethoxymethyl)-2-nitrothiopheneHCID 86703858—
Product5-(Diethoxymethyl)-3-methoxy-2-nitrothiopheneHCID 86703859403.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 3-bromo-5-(diethoxymethyl)-2-nitrothiophene (Int. 66) (1 g, 3.22 mmol) in MeOH (10 ml) copper(II) oxide (0.051 g, 0.645 mmol), KI (10.7 mg, 0.064 mmol) and sodium methanolate (0.662 g, 12.25 mmol) were added, and the mixture was heated under MW irradiation at 120° C. for 2 hours. The reaction mixture was filtered through a celite pad, the filtrate was concentrated under vacuum and then partitioned between 0.5N HCl and EtOAc. The organic phase was dried over sodium sulfate, filtered and evaporated to give 5-(diethoxymethyl)-3-methoxy-2-nitrothiophene (Int. 67) (680 mg, 2.60 mmol, MS/ESI+261.0 [MH]+). This crude was used without any additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440954B2
Source datasetuspto-grants-2016_09
ORD IDord-70e42477b2454f43bc0b4c6e243142dc
Source noteuspto-grants-2016_09