HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl vinyl ether → 4-[2-(1-Ethoxyethoxy)ethoxy]-3,5-dimethoxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl vinyl ether | HCID 8023 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 19622754 | HCID 19622754 | — |
| Reactant | HCID 86642599 | HCID 86642599 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[2-(1-Ethoxyethoxy)ethoxy]-3,5-dimethoxybenzaldehyde | HCID 71427472 | — |
Reaction Steps
To a solution of 4-(2-hydroxyethoxy)-3,5-dimethoxybenzaldehyde (1.5 g, 6.6 mmol) in methylene chloride (22 mL, 0.3 M) was added ethyl vinyl ether (3.4 mL, 19.9 mmol). After addition of PPTS (168 mg, 0.66 mmol), the reaction mixture was stirred for 40 minutes at room temperature. An aqueous saturated sodium hydrogen carbonate solution was added to the reaction fluid, which was then extracted with ethyl acetate, washed with saturated saline, dried over magnesium sulfate, and evaporated under reduced pressure to afford a residue containing an ethoxyethyl-protected 4-(2-hydroxyethoxy-3,5-dimethoxybenzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08178727B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-7388324ef0c84a059209803809dc1cdd |
| Source note | uspto-grants-2012_05 |