HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylcyclohexanol → 4-t-Butylcyclohexyl chlorooxalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylcyclohexanol | HCID 7391 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Product | 4-t-Butylcyclohexyl chlorooxalate | HCID 19612323 | 95.3% |
Reaction Steps
In this example the product was prepared in two synthetic steps. In the first step 4-t-butylcyclohexanol 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 4-t-butylcyclohexyl chlorooxalate having an assay of 96.9% and in a corrected yield of 95.3%. In the second step 4-t-butylcyclohexyl chlorooxalate was reacted with 2,5-dimethyl-2,5-dihydroperoxyhexane, in the presence of pyridine, to yield the product:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05837782 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-75e2af5e52be4f0e9df3825b3c5143e7 |
| Source note | uspto-grants-1998_11 |