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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440225Generated: October 30, 2026

HCID 14702771, compound → HCID 22406459, compound

https://huagongshe.com/reaction/440225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 14702771HCID 14702771—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
ProductHCID 22406459HCID 2240645958%

Reaction Steps

A mixture of (±)-E-4-hydroxy-4-(5-hydroxy-3-methylpent-3-en-1-ynyl)-3,3,5-trimethylcyclohexanone (2.0 g, 8.0 mol), manganese dioxide (14 g, 160 mmol), and acetone (50 mL) were combined and strred for 1.5 h. The mixture was filtered, the solvent removed by evaporation, and the residue chromatographed over silica eluting with 75% ether and 25% hexane to afford 1.17 g (±)-E-4-hydroxy-4-(5-oxo-3-methylpent-3-en-1-ynyl)-3,3,5-trimethylcyclohexanone (58%), as an oil, that gave ir: 3600 (strong), 220 (weak), 1710, 1660, 900 cm-1; gc/eims: 248 (M+, 15%) 233 (9), 219 (19), 205 (16), 192 (42), 163 (95) and 121 (100); 1H nmr -∥: 0.99 and 1.20 (s, gem CH3, 6H), 1.14 (d, J=5.9 Hz, HCCH3, 3H), 2.11 (dd, J=14.3, 2.3 Hz, H-2 eq, 1H), 2.18 (m, H-6eq, 1H), 2.3 (m, 2H), 2.32 (d, J=1.5 Hz, =CCH3, 3H), 2.60 (d, J=14.3 Hz, H-2ax, 1H), 6.22 (dq, J=7.7, 1.5 Hz, =CH, 1H), and 10.03 (d, J=7.7 Hz, CHO, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05518995
Source datasetuspto-grants-1996_05
ORD IDord-1d573a9c175d434192ab4d8aac9837b7
Source noteuspto-grants-1996_05