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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355534Generated: November 1, 2026

(2-Chloro-6-methoxypyridin-4-yl)methanol → 2-Chloro-6-methoxypyridine-4-carbaldehyde

https://huagongshe.com/reaction/1355534

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloro-6-methoxypyridin-4-yl)methanolHCID 11457961—
ReactantHCID 178418287HCID 178418287—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product2-Chloro-6-methoxypyridine-4-carbaldehydeHCID 2762976—

Reaction Steps

To a solution of (2-chloro-6-methoxypyridin-4-yl)methanol (1.73 g, 9.97 mmole) from the protocol immediately above in CH2Cl2 (40 mL) was added PCC (2.58 g, 11.96 mmole) all at once at RT. After 60 hr the mixture was diluted with Et2O and filtered through a plug of Celite®. The filtrate was concentrated to give the titled compound as a tan-yellow solid which was sufficiently pure for use in the next step. 1H-NMR (500 MHz, CDCl3) δ 9.96 (s, 1 H), 7.32 (s, 1 H), 7.06 (s, 1 H), 4.00 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06586424B2
Source datasetuspto-grants-2003_07
ORD IDord-553b57b97ac6411eabc6f77ea68f8657
Source noteuspto-grants-2003_07