HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → Di-t-Butyl Diperoxyfumarate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | tert-Butyl hydroperoxide | HCID 6410 | — |
| Reactant | Fumaryl chloride | HCID 5325504 | — |
| Reactant | Peroxyfumarate | HCID 131720069 | — |
| Solvent | Alpha-Methylstyrene | HCID 7407 | — |
| Product | Di-t-Butyl Diperoxyfumarate | HCID 5880646 | — |
Reaction Steps
Since the actual yield and the actual Act[O] were 38.0 g and 7.31%, respectively, the uncorrected yield was 77.2% and the yield corrected for Act[O] (i.e., the corrected yield) was 79.1%. The higher than expected Act[O] indicated that t-butyl hydroperoxide was somewhat more reactive towards fumaryl chloride than the n-butanol was. The first peroxyfumarate composition (Preparation 1) was found to have a half-life of 19.0 hours at 100° C. in alpha-methylstyrene based on conventional determination procedures.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05644004 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-2c441b6fc7d14d1cae613410fbc302b3 |
| Source note | uspto-grants-1997_07 |