Reaktion #73256

ord-0cc651ffbc07409e81c77f88ad3499c1

Reaktionsgleichung

O=Cc1cc(Br)cs1
4-bromothiophene-2-carbaldehyde
CCO
ethanol
[Cl-].[NH4+]
ammonium chloride
CCOC([O-])[O-]
ethyl orthoformate
CCOC(OCC)c1cc(Br)cs1
4-bromo-2-(diethoxymethyl)thiophene
Ausbeute 81.0%

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe reaction was quenched with water
  2. 2
    Extraktionextracted with ethyl acetate
  3. 3
    WaschenThe combined organic layer was washed with saturated sodium chloride
  4. 4
    Trocknendried over magnesium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated

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): 7.22 (s, 1H), 6.99 (s, 1H), 5.68 (s, 1H), 3.63 (q, 4H) 1.24 (t, 6H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541425B2uspto-grants-2013_09