Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112232Generated: October 30, 2026

Sodium Hydroxide → HCID 53673369, compound

https://huagongshe.com/reaction/1112232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 70622300HCID 70622300—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 53673369HCID 53673369—

Reaction Conditions

Temperature0 °C

Reaction Steps

10 g. of p-ethylphenyl 3,4,7-trimethyl-2,6-nonadienyl ether are dissolved in 110 ml. of dichloromethane and treated portionwise at -10° C. with 7.8 g. of 80% m-chloroperbenzoic acid. After completion of the treatment, the mixture is stirred for a further 2 hours at 0° C., shaken out with 10% sodium sulfite solution, 1-N sodium hydroxide solution and water, dried over sodium sulfate and evaporated. There is obtained pure 6,7-epoxy-1-(p-ethylphenoxy)-3,4,7-trimethyl-2-nonene; NMR (CDCl3): 7.25-6.7 ppm (AB-quartet of the four aromatic protons); 5.5 ppm (a vinyl proton at C-2); 4.52 ppm doublet of the --O--CH2 group); 2.59 ppm (quartet of the aromatic-bound --CH2 group); 2.8-2.2 ppm (multiplet of the protons at C-4 and C-6); 1.65 ppm (wide singlet of the methyl group at C-3); 1.78-0.8 ppm (complicated multiplet of 19 protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04120974
Source datasetuspto-grants-1978_10
ORD IDord-07a4e086ac224660bf19ce720d94adb5
Source noteuspto-grants-1978_10