Reaktion #69226
ord-9c7dc7f272d74b8fa26ea2c736107aea
Reaktionsgleichung
4-bromothiophene-2-carbaldehyde
ethanol
ammonium chloride
ethyl orthoformate
→
4-bromo-2-(diethoxymethyl)thiophene
Ausbeute 81.0%
Reagenzien
Keine
Reaktionsbedingungen
Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe reaction was quenched with water
- 2Extraktionextracted with ethyl acetate
- 3WaschenThe combined organic layer was washed with saturated sodium chloride
- 4Trocknendried over magnesium sulfate
- 5Filtrationfiltered
- 6Einengenconcentrated
Vorschrift
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)thiophene 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).