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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1764169Generated: November 2, 2026

Methanesulfonic Acid → HCID 20306810, compound

https://huagongshe.com/reaction/1764169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantHCID 20306806HCID 20306806—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
ProductHCID 20306810HCID 20306810—

Reaction Steps

The catalytic hydrogenation of the carbonyl group in 2-methyl-2-(t-butylperoxy)-5-hexanone was carried out by shaking 5.0 g. (0.025 mole) of the ketone in a Parr Hydrogenation Apparatus with 25 ml. of 10% methanesulfonic acid solution and 1.0 g. of 5% platinum on carbon catalyst at 0° C. for 2 1/2 hours with a hydrogen pressure of 60 p.s.i.g. At the end of the reaction time, the catalyst was separated by filtration, the product taken up in 50 ml. of pentane, the pentane solution washed to neutrality with water, dried over anhydrous magnesium sulfate and the pentane removed under reduced pressure. The recovered product weighed 3.3 g. (65% recovery). An infrared spectrum showed the presence of a hydroxyl band and the absorption band at 880 cm-1 typical of the t-butylperoxy group.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04115455
Source datasetuspto-grants-1978_09
ORD IDord-cbcd5c01afce4b0b8dd1363e74102920
Source noteuspto-grants-1978_09