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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099570Generated: November 1, 2026

m-Formylbenzonitrile → HCID 68801860, compound

https://huagongshe.com/reaction/2099570

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-FormylbenzonitrileHCID 90670—
Reactant4-Iodo-2-(methylthio)pyrimidineHCID 3858901—
ReactantHCID 178418918HCID 178418918—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68801860HCID 68801860—

Reaction Steps

To the solution of 4-iodo-2-(methylthio)pyrimidine (2.52 g, 10 mmol) in THF (50 mL) at 0 ° C. was added i-PrMgCl (5 mL, 2.0 M, 10 mmol) and stirred for 1 h. 3-cyanobenzaldehyde (1.31 g, 10 mmol) was added. The mixture was stirred at 0° C. for 2 h. The reaction was quenched with saturated aqueous NH4Cl solution and extracted with CH2Cl2. The combined organic layer was dried, filtered, and concentrated. The residue was purified by silica gel chromatography (20-50% EtOAc in hexane) to give 3-{hydroxy[2-(methylthio)pyrimidin-4-yl]methyl}benzonitrile. 1H-NMR (500 MHz, CDCl3) δ 8.46 (d, 1H, J=5.1), 7.72 (s, 1H), 7.65 (d, 1H, J=7.9), 7.61 (d, 1H, J=7.8), 7.48 (t, 1H, J=7.6), 6.84 (d, 1H, J=5.1), 5.69 (d, 1H, J=3.7), 4.58 (d, 1H, J=4.1), 2.60 (s, 3H). LRMS m/z (M+H) Calcd: 258.3, found: 258.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569589B2
Source datasetuspto-grants-2009_08
ORD IDord-46f2e68ac142471487fa4f6544c690c9
Source noteuspto-grants-2009_08