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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635074Generated: October 26, 2026

Sodium borohydride → (2-Fluoro-4-iodopyridin-3-yl)methanol

https://huagongshe.com/reaction/1635074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Fluoro-4-iodopyridine-3-carbaldehydeHCID 9992328—
SolventTetrahydrofuranHCID 8028—
Product(2-Fluoro-4-iodopyridin-3-yl)methanolHCID 11021396—

Reaction Steps

0.72 g (19.2 mmol) of sodium borohydride is added to a solution of 4 g (16 mmol) of 2-fluoro-4-iodo-3-pyridinecarbaldehyde (described in J.O.C., 1993, 58, pp.7832) in 100 ml of tetrahydrofuran. The mixture is stirred at room temperature for 4 hours and then hydrolysed. The reaction mixture is extracted with ethyl acetate. The organic phases are dried and concentrated to yield the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509345B2
Source datasetuspto-grants-2003_01
ORD IDord-f88a3a889058450d9a1fa760030c2add
Source noteuspto-grants-2003_01