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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720114Generated: October 25, 2026

tert-Butyl hydroperoxide → (3-Chloro-2,4,6-trimethylbenzoyl)diphenylphosphine oxide

https://huagongshe.com/reaction/1720114

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl hydroperoxideHCID 6410—
ReactantAcetylacetonateHCID 5460482—
Reactantalpha-Hydroxy-(3-chloro-2,4,6-trimethylbenzyl)-diphenyl phosphine oxideHCID 86749383—
CatalystSodium orthovanadateHCID 61671—
SolventChlorobenzeneHCID 7964—
Product(3-Chloro-2,4,6-trimethylbenzoyl)diphenylphosphine oxideHCID 2242031181%

Reaction Steps

To 15.4 g (0.04 mol) of α-hydroxy-(3-chloro-2,4,6-trimethylbenzyl)-diphenyl phosphine oxide and 0.4 S (1.5mmol) of vanadyl (IV) bis-acetylacetonate in 100 g of chlorobenzene there were added 8.2 g (0.06 mol) of 70w t% strength aqueous tert-butylhydroperoxide and isolated by crystallization following a period of 20 h. Yield: 81%, mp 125°-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504236
Source datasetuspto-grants-1996_04
ORD IDord-c6407c3bd2cd4c85aaffa930feb700ae
Source noteuspto-grants-1996_04