HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Dimethylphenol → Methyl 2,6-dimethylphenoxy acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Dimethylphenol | HCID 11335 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2,6-dimethylphenoxy acetate | HCID 13966814 | — |
Reaction Steps
65 g of 2,6-dimethylphenol are dissolved in 200 ml of dry DMF and, under N2, 23.2 g of a 55% suspension of sodium hydride in mineral oil are added in portions. Then 50.4 ml of methyl bromoacetate are added dropwise with stirring, and the mixture is left to stand overnight. The precipitated salt is filtered off with suction, and the filtrate is concentrated. The residue is taken up in ethyl acetate, and the solution is extracted with water. The organic phase is dried over magnesium sulfate and concentrated. An oily liquid remains and is used directly in the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04922015 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-abb667927a7d48738b99f839806d3a18 |
| Source note | uspto-grants-1990_05 |