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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661854Generated: October 25, 2026

Trimethylolpropane diallyl ether → [3-(2-Hydroxymethyl-2-{3-[hydroxy-(2,4,4-trimethylpentyl)-phosphinoyl]-propoxymethyl}-butoxy)-propyl]-(2,4,4-trimethylpentyl)-phosphinic acid

https://huagongshe.com/reaction/1661854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylolpropane diallyl etherHCID 61196—
ReactantHCID 178460681HCID 178460681—
CatalystDi-tert-amyl peroxideHCID 25320—
Product[3-(2-Hydroxymethyl-2-{3-[hydroxy-(2,4,4-trimethylpentyl)-phosphinoyl]-propoxymethyl}-butoxy)-propyl]-(2,4,4-trimethylpentyl)-phosphinic acidHCID 57909086100.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

10 g (0.056 moles) of 2,4,4-trimethylpentyl phosphinic acid, 6.01 g (0.028 moles) of trimethylolpropane diallyl ether and 0.4 mL (0.0019 moles) of di-tert-amylperoxide are mixed in a 100 mL single neck flask. The mixture is purged with argon to remove oxygen and is heated under argon for 6 hours at 140° C. Tert-amyl alcohol is removed by distillation and 16 g (quantitative yield) of [3-(2-hydroxymethyl-2-{3-[hydroxy-(2,4,4-trimethylpentyl)-phosphinoyl]-propoxymethyl}-butoxy)-propyl]-(2,4,4-trimethylpentyl)-phosphinic acid is obtained as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030435B2
Source datasetuspto-grants-2011_10
ORD IDord-32b83ec0f54242348999164dcb2f3216
Source noteuspto-grants-2011_10