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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1066896Erstellt: 26. Oktober 2026

5-Bromo-2-methoxybenzaldehyde → HCID 19379069, Verbindung

https://huagongshe.com/reaction/1066896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Bromo-2-methoxybenzaldehydeHCID 90684—
EduktCyclopentyltriphenylphosphonium bromideHCID 2735896—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 19379069HCID 1937906984,5%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

n-BuLi (1.6M solution in hexane) (72.5 ml, 116 mmol) was added dropwise at 0° C. to a solution of cyclopentyltriphenylphosphonium bromide (45.8 g, 111 mmol) in THF (300 ml). The red solution was stirred at 0° C. for 0.5 h then treated with a solution of 5-bromo-2-methoxybenzaldehyde (23.5 g, 109 mmol) in THF (150 ml). The reaction mixture was stirred at RT overnight, concentrated in vacuo, then partitioned between CH2Cl2 (250 ml) and water (150 ml). The organic phase was separated and combined with further CH2Cl2 extracts (2×50 ml). The organic phase was washed (brine; 50 ml), dried (Na2SO4), and concentrated in vacuo. The residue was subjected to chromatography (SiO2; CH2Cl2) to afford the title compound (24.6 g), as a colourless oil δH (80 MHz; CDCl3) 1.6-1.9 (4H, br m, CH2(CH2)2), 2.3-2.6 (4H, br m, CH2(CH2)2CH2), 3.76 (3H, s, OMe), 6.4-6.5 (1H, br m, CH═C), 6.65 (1H, d, J 8.5 Hz, ArH ortho to OMe), 7.18 (1H, dd, J 8.5, 2.4 Hz, ArH para to olefin), and 7.39 (1H, d, J 2.4 Hz, ArH ortho to olefin).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06245774B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-983e9cea9e384e9c8b092cbe776e7a7e
Quellennotizuspto-grants-2001_06