HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658032Generated: October 25, 2026
Trilauryl phosphite → Di-n-dodecyl 4-tert.-butyl-2,6-dimethyl-3-hydroxybenzylphosphonate
https://huagongshe.com/reaction/1658032
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trilauryl phosphite | HCID 76495 | — |
| Reactant | 6-tert-Butyl-3-(chloromethyl)-2,4-dimethylphenol | HCID 90131 | — |
| Product | Di-n-dodecyl 4-tert.-butyl-2,6-dimethyl-3-hydroxybenzylphosphonate | HCID 21311762 | — |
Reaction Steps
41 Grams of trilauryl phosphite and 16.1 grams of 6-tert.-butyl-3-chloromethyl-2,4-dimethylphenol were stirred together as a melt at 105° to 110° for 1 hour, followed by 110° to 120° for 2 hours, 120° to 125° for 10 hours and finally at 140° to 145° for 4 hours. The crude was topped in the "ASCO 50" Rotafilm Molecular Still at a wall temperature of 80° to 90° at 1 to 5 microns Hg. pressure to remove most of the by-product dodecyl chloride as well as small amounts of other volatiles. This topping procedure was repeated at a wall temperature of 200° to 210° at the same pressure to remove additional volatiles. The desired product distilled at a wall temperature of 250° to 260° at 1 micron Hg. pressure yielding the desired product as a colorless liquid which solidified to a white solid (m.p. 36° to 42°). (compound 3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03962376 |
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| Source dataset | uspto-grants-1976_06 |
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| ORD ID | ord-b2e5072362264fe78c0a76b00ab98b7a |
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| Source note | uspto-grants-1976_06 |
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