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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515146Generated: October 27, 2026

4,4-Dimethylpent-2-yn-1-ol → 4,4-Dimethyl-1-pentanol

https://huagongshe.com/reaction/515146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-Dimethylpent-2-yn-1-olHCID 11789162—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4,4-Dimethyl-1-pentanolHCID 18393—
Product4,4-DimethylpentanalHCID 11062343—

Reaction Steps

To a stirred solution of 4,4-dimethyl-pent-2-yn-1-ol (3.1 g, 27.6 mmol) in ethanol (30 ml) is added 10% palladium on carbon (0.3 g). The mixture is stirred under an atmosphere of hydrogen for 16 h. The reaction mixture is filtered through a pad of celite and the celite bed is washed with methanol (10 ml). The filtrate thus obtained is concentrated and the crude product is purified by column chromatography (5-10% ethyl acetate/hexane) to afford 4,4-dimethyl-pentan-1-ol and 4,4-dimethyl-pentan-1-al. To a stirred solution of 4,4-dimethyl-pentan-1-al (0.85 g, 7.45 mmol) in methanol (12 ml) is added sodium borohydride (0.56 g, 14.9 mmol) at 0° C. The reaction mixture is stirred at RT for 1.5 h. On completion, the solvent is evaporated and then diluted with ethyl acetate (30 ml). The organic layer is washed with water (2×20 ml), brine (20 ml), dried over sodium sulfate and concentrated affording 4,4-dimethyl-pentan-1-ol (1.52 g, 13.1 mmol, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-36e5fc7b903e454aa4afd404b2ce3c98
Source noteuspto-grants-2015_08