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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169998Generated: October 25, 2026

Salicylaldehyde → HCID 53250564, compound

https://huagongshe.com/reaction/2169998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
Reactant2-Amino-6-methoxypyridineHCID 580053—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53250564HCID 53250564—

Reaction Steps

512 mg (2.41 mmol, 1.5 eq) of sodium triacetoxyborohydride are added to a solution of 200 mg (1.61 mmol, 1 eq) of 6-methoxypyridin-2-ylamine (starting material 1) and 236 mg (2.41 mmol, 1 eq) of 2-hydroxybenzaldehyde (starting material 2) in 20 ml of tetrahydrofuran. The solution is stirred at room temperature for 48 h. It is evaporated and the residue is taken up in 100 ml of dichloromethane and then extracted with a saturated aqueous solution of ammonium chloride. The aqueous phase is extracted twice with dichloromethane. The organic phases are combined and dried over sodium sulphate. The residue is chromatographed on silica gel (5/95 ethyl acetate/heptane). 2-[(6-methoxypyridin-2-ylamino)methyl]phenol is obtained in the form of a white solid. Melting point=103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09050266B2
Source datasetuspto-grants-2015_06
ORD IDord-eb5da2db59fa4c4ba1211fd2a8aac93e
Source noteuspto-grants-2015_06