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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371965Generated: October 25, 2026

2,2,6-Trimethylcyclohexanone → Tetramethyl-cyclohexanone

https://huagongshe.com/reaction/371965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,6-TrimethylcyclohexanoneHCID 17000—
Reactant2,2,3,6-Tetramethylcyclohexan-1-olHCID 19910535—
ProductTetramethyl-cyclohexanoneHCID 22644489—

Reaction Steps

If the procedure of Example 8 is followed but instead of 28 g of 2,2,6-trimethyl-cyclohexanone 31 g of 2,2,3,6-tetramethyl-cyclohexanol are employed, fractional distillation gives 9.6 g of unconverted tetramethyl-cyclohexanone and 21 g (corresponding to 73% of theory, based on ketone converted) of 2,2,3,6-tetramethyl-1-(but-1'-yn-3'-en-1'-yl)-cyclohexanol of boiling point 66°-67° C/0.2 mm Hg and refractive index nD25 = 1.5018. Fragrance note: faintly floral, coniferous, fruity.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04088681
Source datasetuspto-grants-1978_05
ORD IDord-307b71d4dda84a05a97ec712f46ba46b
Source noteuspto-grants-1978_05