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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12596Generated: October 26, 2026

Sodium Hydroxide → HCID 178447302, compound

https://huagongshe.com/reaction/12596

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67245353HCID 67245353—
ReactantHCID 178514830HCID 178514830—
CatalystHCID 178418476HCID 178418476—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 178447302HCID 17844730285.1%

Reaction Conditions

Temperature70 °C

Reaction Steps

Nitrogen is bubbled for 5 min. To a mixture made up of 0.20 g (0.48 mmol) of N-(4-iodobenzyl)-N-valeryl-L-valine, 0.115 g (0.61 mmol) of 2-(1H-tetrazol-5-yl)phenylboronic acid, 0.017 g (0.024 mmol) of bis(triphenylphosphine)palladium chloride and 0.115 g (2.87 mmol) of NaOH in 2.4 mL of methanol and 0.7 mL of water are added. The reaction is heated to 70° C. under nitrogen atmosphere. Once 3 h has elapsed the reaction is considered to be completed and the methanol is distilled. The crude product is treated with 25 mL of HCl 1N and 25 mL of AcOEt. The AcOEt phase is dried with anhydrous sodium sulphate and after distilling the solvent the crude product obtained is purified by silica gel chromatography (eluent AcOEt/heptane/AcOH 1.5:5:0.2) to provide 0.178 g (85%) of Valsartan.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728021B2
Source datasetuspto-grants-2010_06
ORD IDord-2c34eba3d0b341ddb43c12b392296d96
Source noteuspto-grants-2010_06