HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenyl phosphite → Phosphite
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenyl phosphite | HCID 7540 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 54336092 | HCID 54336092 | — |
| Product | Phosphite | HCID 107908 | — |
| Product | HCID 18513237 | HCID 18513237 | — |
Reaction Steps
Bis (tetrahydroabietyl 2,4 di-tert-butyl phenyl) phosphite was prepared by first reacting 206 g (1 mol) of 2,4 di-tert-butylphenyl phenol with 310 g (1 mol) of triphenyl phosphite catalyzed with 2 g of sodium methylate (or phenate) to obtain a nominal 2,4 di-tert-butylphenyl diphenyl phosphite. Phenol was distilled through a 20 cm. Raschig ring packed column to 150° C. and 30 mm. The reaction terminates at 190° C. at 4 mm after distilling the calculated 1 mol of phenol. The product mixture contained approximately 85% of the desired 2,4,di-tert-butylphenyl diphenylphosphite. The remainder was identified as being predominantly a mixture of bis (2,4 -di-tert-butylphenyl) phenyl phosphite and unreacted triphenyl phosphite.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05141975 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-2c0fd045a69641c6bfd5c3b6773864ac |
| Source note | uspto-grants-1992_08 |