Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boric Acid | HCID 7628 | — |
| Reactant | Dodecylamine | HCID 13583 | — |
| Reactant | 2-(4-Methylphenyl)oxirane | HCID 108111 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13390906 | HCID 13390906 | — |
Reaction Steps
The boramid compound, 1-hydroxy-4,6-dicresyl-5-dodecyl-5-aza-1-bora-2,8-dioxacyclooctane is prepared by adding 21 grams of boric acid with 61.7 grams of dodecylamine, 89.3 grams of para methylstyrene oxide and 250 ml of toluene to a single necked one liter round-bottomed flask. The toluene acts as a solvent and as an azeotrope for water produced during the reaction. It should be noted that boric acid is not soluble in toluene. The flask is placed in a heating mantle and fitted with a Dean Stark trap that is topped with a water-cooled condenser. The mixture thus formed is heated until it begins to reflux. Next, the mantle heat is adjusted to give a moderate reflux rate. The reaction mixture is refluxed for one hour, or until the stoichiometric amount of water (12 ml) collects in the Dean-Stark trap and all of the boric acid has dissolved, after which the toluene is distilled from the reaction product. The reaction produces 160 grams of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04511516 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-1d0c4deac1ae4e94a0aab5d681efad58 |
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| Source note | uspto-grants-1985_04 |
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