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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075367Generated: October 29, 2026

Cyclohexene → HCID 15383566, compound

https://huagongshe.com/reaction/1075367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexeneHCID 8079—
ReactantHCID 15383567HCID 15383567—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 15383566HCID 1538356678.6%

Reaction Steps

A mixture of the above crude oil of benzyl 2-hydroxy-3-[2-methyl-3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]propyl]benzoate (11.61 g, 0.023 mol), ethanol (40 ml), cyclohexene (12 ml) and 10% palladium-on-charcoal (1.2 g) was maintained at reflux for 1 hour. The mixture was cooled and rinsed with ethanol. The liquids were concentrated and the pale yellow oil obtained was purified by chromatography on silica under pressure (eluent: 80/20/0.2 CH2Cl2 /ethyl acetate/acetic acid) to give 7.5 g (yield: 78%) of 2-hydroxy-3-[2-methyl-3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]-propyl]benzoic acid in the form of a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05900231
Source datasetuspto-grants-1999_05
ORD IDord-4e2d77a2be93472c969df6e25e9833a0
Source noteuspto-grants-1999_05