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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817595Generated: October 29, 2026

Ethanol → 4-Bromo-2-(diethoxymethyl)thiophene

https://huagongshe.com/reaction/1817595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
ReactantEthylorthoformateHCID 53630039—
Product4-Bromo-2-(diethoxymethyl)thiopheneHCID 1228002481%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 4-bromothiophene-2-carbaldehyde (1.2 g, 0.0063 mol) in ethanol (10 mL, 0.2 mol) was treated with ammonium chloride (0.42 g, 0.0078 mol) and ethyl orthoformate (1.2 g, 0.0078 mol). The mixture was stirred at 60° C. for 2 hours. The reaction was quenched with water and extracted with ethyl acetate. The combined organic layer was washed with saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated to give 4-bromo-2-(diethoxymethyl)thio-phene as an oil (1.3 g, 81% ). 1H NMR (400 MHz, CDCl3): δ 7.22 (s, 1H), 6.99 (s, 1H), 5.68 (s, 1H), 3.63 (q, 4H) 1.24 (t, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598257B2
Source datasetuspto-grants-2009_10
ORD IDord-9a893d45c4cd4192bed63dd71ad4ce80
Source noteuspto-grants-2009_10