HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → Ethyl 2-(3-formylphenoxy)-2-methylpropanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Propanoic acid, 2-bromo-2-methyl-, ethyl ester | HCID 11745 | — |
| Reactant | HCID 178474001 | HCID 178474001 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 2-(3-formylphenoxy)-2-methylpropanoate | HCID 18766496 | 59% |
Reaction Steps
In an ethanol solvent, 1 N ethoxy sodium (NaOEt) (1.1 eq.) was added dropwise to 3-hydroxybenzaldehyde (1.0 eq.) and ethyl α-bromoisobutyrate (1.1 eq.), and the reaction mixture was refluxed. After the ethanol was evaporated, the residual was distributed between ethyl acetate and water, and an organic layer was dried by using MgSO4, filtered, and evaporated. The residual was purified by silica gel column chromatography using hexane and ethyl acetate (8:1) to obtain Compound 97b.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08889881B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-260700aeb1964f25b3cb00c457eeec55 |
| Source note | uspto-grants-2014_11 |