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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622863Generated: October 31, 2026

Peracetic Acid → HCID 14274524, compound

https://huagongshe.com/reaction/622863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPeracetic AcidHCID 6585—
ReactantSodium AcetateHCID 517045—
ReactantHCID 14274523HCID 14274523—
ReactantHCID 18945546HCID 18945546—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductHCID 14274524HCID 1427452498%

Reaction Conditions

Temperature41 °C

Reaction Steps

To show another example of the epoxy-sulfonylazide of the instant invention, a solution of p-methallyloxybenzenesulfonylazide (506 parts) in methylene chloride (1,450) parts is stirred and heated to reflux (41° C.) then a solution of 35% peracetic acid in acetic acid (521.5 parts) containing sodium acetate (15.6 parts) is added slowly from an addition funnel over 15 minutes. An additional 40 parts of methylene chloride is added to adjust the reflux temperature to 45° C. After 6 hrs stirring and refluxing at 45° C. the reaction is quenched with 835 parts of distilled water. The layers are separated and the organic phase is washed with 555 parts of 10% sodium sulfite, 835 parts of sodium bicarbonate, and 565 parts of distilled water containing 23 parts of trioctylammonium chloride. The solution is dried azeotropically, and the solvent is removed at 55° C. and 20 mm to yield 528 parts of 3-(p-azidosulfonylphenoxy)-2-methylpropylene oxide as a white, crystalline solid. This represents a yield of 98%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772733
Source datasetuspto-grants-1988_09
ORD IDord-443c751736064562ae142a09aaeeb97d
Source noteuspto-grants-1988_09