HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → benzyl chlorooxalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Product | benzyl chlorooxalate | HCID 11019858 | 92.1% |
Reaction Steps
In this example the product was prepared in two synthetic steps. In the first step benzyl alcohol was reacted with 50% molar excess of oxalyl chloride. Upon completion of the reaction the excess oxalyl chloride was stripped from the product at reduced pressure to produce benzyl chlorooxalate having an assay of 96.6% and in a corrected yield of 92.1%. In the second step benzyl chlorooxalate was reacted with 2,5-dimethyl-2,5-dihydroperoxyhexane, in the presence of pyridine, to yield the product as described below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837782 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-3b33bdba8e36490c84e99bd7a4585c12 |
| Source note | uspto-grants-1998_11 |