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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 501732Erstellt: 24. Oktober 2026

3-Hydroxybenzaldehyde → 3-Isopropoxybenzaldehyde

https://huagongshe.com/de/reaction/501732

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-HydroxybenzaldehydeHCID 101—
EduktIsopropyl iodideHCID 6362—
EduktPotassium CarbonateHCID 11430—
Edukt(S)-2,2,2-trifluoro-N-(6-methoxy-3-oxo-2,3-dihydro-1H-inden-1-yl)acetamideHCID 1472787—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-IsopropoxybenzaldehydeHCID 71291485%

Reaktionsschritte

Step AU (1). A solution of 3-hydroxybenzaldehyde (67 g, 549 mmol), 2-iodopropane (100 g, 588 mmol) and K2CO3 (130 g, 942 mmol) in 400 mL DMF was stirred for 18 h. To the above solution was added 2-iodopropane (20 g, 117 mmol) and K2CO3 (20 g, 145 mmol) and the mixture was stirred for another 24 h. The reaction mixture was poured into 300 mL water which was extracted with EtOAc (200 mL×3). The combined organic layers were washed with water (100 mL×3), dried over Na2SO4, filtered, and concentrated in vacuo to afford 77 g (85% yield) of 3-isopropoxybenzaldehyde as an oil. 1H NMR (300 MHz, CDCl3) δ 1.29-1.31 (d, 6H) 4.5-4.6 (m, 1H) 7.0-7.1 (m, 1H) 7.3-7.4 (m, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07772221B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-8571272274344ffcbf958067fbe99d83
Quellennotizuspto-grants-2010_08