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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18070Erstellt: 23. Oktober 2026

6-Chloropyridine-3-carbaldehyde → 2-(Chloropyrid-5-yl)-(4-chlorophenyl)methanol

https://huagongshe.com/de/reaction/18070

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Chloropyridine-3-carbaldehydeHCID 2764053—
Edukt2-(Chloropyrid-5-yl)-(4-chlorophenyl)bromomethaneHCID 22506785—
EduktHCID 178478191HCID 178478191—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(Chloropyrid-5-yl)-(4-chlorophenyl)methanolHCID 22506792—

Reaktionsschritte

2-(Chloropyrid-5-yl)-(4-chlorophenyl)bromo-methane may be prepared by carrying out the procedure in a manner similar to Example 84, starting with 22.5 cm3 of 4-chlorophenylmagnesium bromide (1 M solution in ethyl ether) in 30 cm3 of tetrahydrofuran, under an inert argon atmosphere, and 2.9 g of 2-chloropyridine-5-carboxaldehyde in 30 cm3 of tetrahydrofuran. 3.42 g of 2-(chloropyrid-5-yl)-(4-chlorophenyl)methanol are thus obtained in the form of a pale green powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741316B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ce483d21a0764f32b303eb4437437310
Quellennotizuspto-grants-2010_06