HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Ethyl triacontanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triacontanoic acid | HCID 10471 | — |
| Product | Ethyl triacontanate | HCID 139039 | — |
Reaction Steps
The acid chloride of 1-triacontanoic acid is converted to the ester by adding methanol or ethanol and stirring for 1/2 to 1 hour. The alcohol was evaporated on a rotary evaporator leaving ethyl-1-triacontanoate. The ester is then reacted in a pressure vessel under about 250 atmospheres of hydrogen in the presence of a powdered copper chromite catalyst for about 12 hours at 250° C. to produce 1-triacontanol. One part of catalyst is present for every 5 to 10 parts of ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04167641 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-d47b311755e54f8f8eb9f6e6499002bd |
| Source note | uspto-grants-1979_09 |