Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 5,7,7-Trimethyl-2-(1,3,3-trimethylbutyl)-1-octanol | HCID 256371 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86609193 | HCID 86609193 | 34.7% |
Reaction Steps
With nitrogen substitution, 540 ml of toluene and 138.0 grams (0.9 moles) of phosphorus oxychloride were added and cooled to −10 degrees C. To this mixture, a solution of 243.5 grams (0.9 moles; 1.0 in molar ratio) of 2-(1,3,3-trimethyl-n-butyl)-5,7,7-trimethyl-n-octanol and 91.1 grams (0.9 moles) of triethylamine was dripped, and the mixture was reacted for 12 hours at 0 degrees C. The mixture was then heated to 25 degrees C., and a triethylamine hydrochloride was removed by filtering to obtain 1003.9 grams of a toluene solution of [2-(1,3,3-trimethyl-n-butyl)-5,7,7-trimethyl-n-octyl] dichlorophosphate (34.7% in concentration).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569211B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-0075226fa1d548c8a9e773e4d1c863d5 |
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| Source note | uspto-grants-2009_08 |
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