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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylolpropane diallyl ether | HCID 61196 | — |
| Reactant | HCID 178460681 | HCID 178460681 | — |
| Catalyst | Di-tert-amyl peroxide | HCID 25320 | — |
| Product | [3-(2-Hydroxymethyl-2-{3-[hydroxy-(2,4,4-trimethylpentyl)-phosphinoyl]-propoxymethyl}-butoxy)-propyl]-(2,4,4-trimethylpentyl)-phosphinic acid | HCID 57909086 | 100.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030435B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-32b83ec0f54242348999164dcb2f3216 |
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| Source note | uspto-grants-2011_10 |
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