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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 979641Generated: October 29, 2026

Methanol → Perhydroxyl radical

https://huagongshe.com/reaction/979641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
ReactantPeracetic AcidHCID 6585—
ProductAcetic AnhydrideHCID 7918—
ProductPerhydroxyl radicalHCID 1850031%

Reaction Steps

A portion of the beads produced (20 g) were swelled in 60 ml of a solution of dichloromethane and methanol (equal volume ratios) and 80 g of peracetic acid solution obtained from 31% hydroperoxide and acetic anhydride, were added drop by drop with cooling and the reaction was continued for 4 hours at room temperature in order to oxidize triphenylphosphine units. The beads containing triphenylphosphine oxide units were dipped into 100 ml of monochlorobenzene containing 10 g of oxalic chloride and the solution was stirred for 5 hours at room temperature so as to convert triphenylphosphine oxide units into triphenylphosphine dichloride units. The beads were washed with dichloromethane (CH2Cl2) completely and dried. Yield of the beads was 24.9 g. The beads produced contained pendant diphenylphosphine dichloride groups and had the structural formula: ##STR9##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04668762
Source datasetuspto-grants-1987_05
ORD IDord-acea9ff4163142c7805e66d568a9a115
Source noteuspto-grants-1987_05