HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(3-Bromo-4,5-dimethoxyphenyl)-1-ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Bromo-4,5-dimethoxybenzaldehyde | HCID 81379 | — |
| Reactant | HCID 178418689 | HCID 178418689 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Bromo-4,5-dimethoxyphenyl)-1-ethanol | HCID 15173656 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Under nitrogen, a solution of the 3-bromo-4,5-dimethoxybenzaldehyde (2.45 g; 10 mmol) in dry THF (10 ml) was added via syringe through a septum to a cold (ice-bath) solution of MeMgBr (15 mmol; 5.0 ml of 3.0 M Et2O solution) diluted with 10 ml dry THF. After the addition, the mixture was stirred for 10 minutes at 0° C., then for 1 hour at room temperatures. TLC (Hex:EtOAc=3:1) indicated complete disappearance of the reactant and a new product spot with lower Rf (0.25 vs 0.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08637575B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-0bd70144380943f296bfbc856a7dd3fe |
| Source note | uspto-grants-2014_01 |