HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-Ethoxyethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Propanol | HCID 1031 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-Ethoxyethanol | HCID 10129898 | — |
| Product | 2-Propanol, 2-methoxy- | HCID 10887827 | — |
Reaction Steps
The 4,5-diacyl-[1,4,5]-oxadiazepines obtained in this reaction step can be obtained especially by precipitation from alcohols such as methanol, ethanol, propanol, isopropanol, methoxyisopropanol and ethoxyethanol. They are generally obtained in yields of from 40 to 76% and in a purity of more than 95%. It is not necessary, however, to isolate those intermediates; they can be introduced directly into the next step by replacing the solvent of reaction step (1) by the solvent of reaction step (2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07598376B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-225c05a72f1e498a821f8c46e62abc5c |
| Source note | uspto-grants-2009_10 |