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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088489Generated: November 1, 2026

2-Methylenenonanoic acid → 2-Methylnonanoic acid

https://huagongshe.com/reaction/1088489

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylenenonanoic acidHCID 11041145—
ReactantHCID 178418361HCID 178418361—
SolventEthanolHCID 702—
Product2-Methylnonanoic acidHCID 9116698.9%

Reaction Steps

In a 200 ml autoclave, the inside atmosphere of which had previously been replaced with argon, were placed 3.0 g (17.6 mmoles) of 2-methylenenonanoic acid and 50 ml of ethanol. Then, 6.9 mg (0.007 mmole) of [Ru((-)-T-BINAP)](ClO4)2 prepared according to the same manner as in Referential Example 6 except using (-)-T-BINAP in place of (+)-T-BINAP was added to the mixture to perform hydrogenation for 15 hours at a hydrogen pressure of 30 kg/cm2 and at a reaction temperature of 20° C. Thereafter, the solvent was distilled off to provide 3.0 g of 2-methylnonanoic acid. The theoretical yield (hereafter simply referred to as "yield") was 100%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04962230
Source datasetuspto-grants-1990_10
ORD IDord-10351a58b4dc487d98ae959ca3d4e952
Source noteuspto-grants-1990_10