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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18070Generated: October 25, 2026

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

https://huagongshe.com/reaction/18070

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
Reactant2-(Chloropyrid-5-yl)-(4-chlorophenyl)bromomethaneHCID 22506785—
ReactantHCID 178478191HCID 178478191—
SolventTetrahydrofuranHCID 8028—
Product2-(Chloropyrid-5-yl)-(4-chlorophenyl)methanolHCID 22506792—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741316B2
Source datasetuspto-grants-2010_06
ORD IDord-ce483d21a0764f32b303eb4437437310
Source noteuspto-grants-2010_06