HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → Butyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Butyl ether | HCID 8909 | — |
Reaction Steps
1 mole of pyrocatechol or pyrocatechol derivatives (see Table 1) in a mixture of 500 ml of toluene and 50 ml of dioxane was taken and 1.05 mole of oxalyl chloride were added dropwise at 70° C. Thereafter, the mixture was subsequently stirred until the evolution of gas had ended. After the reaction mixture had cooled to room temperature, it was filtered and the solid product was dried in vacuo. The same results were obtained when diethyl ether or dibutyl ether was used instead of the toluene/dioxane mixture. The starting materials and the results are summarized in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04620018 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-ee0eb1786fff45d0bb79baffb2517a5a |
| Source note | uspto-grants-1986_10 |