HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507722Generated: October 26, 2026
Isopropanol → Tris(2,4-DI-tert-butylphenyl)phosphate
https://huagongshe.com/reaction/507722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Tris(2,4-di-tert-butylphenyl) phosphite | HCID 91601 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tris(2,4-DI-tert-butylphenyl)phosphate | HCID 14572930 | — |
Reaction Steps
tris(2,4-Di-tert.butylphenyl)phosphite (5146 g; Irgafos® 168, Ciba Specialty Chemicals) and isopropanol (IPA, 7890 g) are mixed in a reaction vessel and heated to 55-60° C. At this point the mixture is a slurry of approximately 39.0% solids. The peroxide (549 g, 50 weight-% solution of H2O2 in water, 1 equivalent) is added for 2-3 hours while maintaining the pot temperature (reaction is exothermic). After the peroxide addition, the mixture is maintained for 1 hour at 60° C. The reaction mass is homogeneous and the completeness of reaction is checked by LC (>97.0% conversion). Water (1355 g) is added, and the reaction mass is seeded to induce crystallization. Cooling slowly in 2 steps to 45° C. and then to 20° C. completes crystallization. The product is filtered (25μ screen), then dried at 70° C. under full vacuum with a nitrogen sweep.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786199B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-56e34206602e4b4e8d3e1d57e57be77b |
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| Source note | uspto-grants-2010_08 |
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