HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-[2-(Benzyloxycarbonyl)ethoxy]-2-methylbenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Carboxyethoxy)-2-methylbenzaldehyde | HCID 23077858 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(Benzyloxycarbonyl)ethoxy]-2-methylbenzaldehyde | HCID 85938873 | — |
Reaction Steps
To a suspension of 4-(2-carboxyethoxy)-2-methylbenzaldehyde (7.2 g) and potassium carbonate (14.3 g) in N,N-dimethylformamide (70 mL) was added benzyl bromide (8.2 mL) at room temperature, and the mixture was stirred overnight. The reaction mixture was poured into water, and the resulting mixture was extracted with diethyl ether. The extract was washed with water and brine, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=4/1-3/1) to give the title compound (6.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375087B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-3c8b39f77bd6423192d1a504e5a48c81 |
| Source note | uspto-grants-2008_05 |