HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155264Generated: November 1, 2026
Dibutylamine → Dibenzo[d,f][1,3,2]dioxaphosphepin-6-amine, N,N-dibutyl-2,4,8,10-tetrakis(1,1-dimethylethyl)-
https://huagongshe.com/reaction/1155264
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | 3,3',5,5'-Tetrakis(1,1-dimethylethyl)(1,1'-biphenyl)-2,2'-diol | HCID 80808 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Dibenzo[d,f][1,3,2]dioxaphosphepin-6-amine, N,N-dibutyl-2,4,8,10-tetrakis(1,1-dimethylethyl)- | HCID 20481433 | — |
Reaction Steps
170 g (0.414 mol) of 4,4',6,6'-tetra-tert-butyl-2,2'-biphenol in 150 ml of toluene is heated to 80°-90° C. in a nitrogen atmosphere, and 40 ml (0.458 mol) of phosphorus trichloride is added dropwise in the course of 2 hours. The reaction mixture is stirred at reflux temperature for 4 hours and, towards the end of the reaction, nitrogen gas is again introduced. There is then added dropwise at reflux temperature, during 11/2 hours, a solution of 53.5 g (0.414 mol) of dibutylamine and 41.9 g (0.414 mol) of triethylamine in 80 ml of toluene. After 15 hours, the reaction mixture is allowed to cool to room temperature, and the triethylamine hydrochloride which has precipitated is filtered off. The toluene is afterwards evaporated off, and the N-(2,4,8,10-tetra-tert-butyl-dibenz[d,f][1,3,2]dioxaphosphepin-6-yl)-dibutylamine obtained has a melting point of 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04301061 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-c5445ce7f13c4717af1e73ae9fdea7fd |
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| Source note | uspto-grants-1981_11 |
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