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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349809Generated: October 26, 2026

Peracetic Acid → 3-((R)-5-Cyclohexyl-3-methyl-pentyl)-2,2-dimethyl-oxirane

https://huagongshe.com/reaction/349809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPeracetic AcidHCID 6585—
ReactantSodium SulfiteHCID 24437—
ReactantSodium BicarbonateHCID 516892—
Reactant(3R)-(3,7-Dimethyl-oct-6-enyl)-cyclohexaneHCID 86597959—
SolventDichloromethaneHCID 6344—
Product3-((R)-5-Cyclohexyl-3-methyl-pentyl)-2,2-dimethyl-oxiraneHCID 86597960—

Reaction Conditions

Temperature0 °C

Reaction Steps

A flask was charged with 11.48 g (51.6 mmol) of crude (3R)-(3,7-dimethyl-oct-6-enyl)-cyclohexane, 100 mL of dichloromethane, and 9.33 g (111 mmol) of sodium bicarbonate. The mixture was cooled in a 0° C. bath. Slowly 11.6 mL (55.2 mmol) 32% peracetic acid was added. The mixture was stirred for 4 hours at 0° C. Then 10% aqueous sodium sulfite was added slowly until bubbling ceased. The layers were separated, and the organic layer was washed twice with 10% aqueous sodium sulfite and dried over magnesium sulfate. The drying agent was removed by filtration, and the solvent was removed under reduced pressure. The remaining residue was 10.65 g (87%) of a clear oil: 1H NMR (400 MHz, CDCl3) ppm 0.86 (m, 5 H) 1.00 (d, J=6.59 Hz, 2 H) 1.14 (m, 7 H) 1.25 (s, 3 H) 1.29 (s, 3 H) 1.35 (m, 2 H) 1.50 (m, 3 H) 1.65 (m, 5 H) 2.68 (td, J=6.16, 1.83 Hz, 1 H). MS (APCl) m+1/z=239.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179934B2
Source datasetuspto-grants-2007_02
ORD IDord-d8143efb73b44a87a86e44918dafc1b8
Source noteuspto-grants-2007_02