HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromooctane → Methyl 3,5-bis(octyloxy)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromooctane | HCID 8140 | — |
| Reactant | Methyl 3,5-Dihydroxybenzoate | HCID 75076 | — |
| Product | Methyl 3,5-bis(octyloxy)benzoate | HCID 20443352 | — |
Reaction Steps
200 ml of ethyl alcohol and then 2.3 g of purified sodium are introduced into a 500 ml Erlenmeyer flask. A reflux condenser is fitted to the Erlenmeyer flask and the reaction medium is stirred with a magnetized bar. When the sodium ethylate is formed, 8.4 g of methyl-3,5-dihydroxybenzoate is added, accompanied by stirring. As soon as the medium has become homogeneous, 20.26 g of distilled octyl bromide are added dropwise. Heating under refluxing takes place for 20 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04474679 |
| Source dataset | uspto-grants-1984_10 |
| ORD ID | ord-b16ab4a2e3744e7ba34e93f3c78411af |
| Source note | uspto-grants-1984_10 |