HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Acetaldehyde, 2-(4-bromo-2-methylphenoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 4-Bromo-1-[(2,2-dimethoxyethyl)oxy]-2-methylbenzene | HCID 19608546 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Acetaldehyde, 2-(4-bromo-2-methylphenoxy)- | HCID 14816015 | 116.6% |
Reaction Steps
A 5N HCl (15 mL) solution is added to a stirred solution of 4-bromo-1-(2,2-dimethoxy-ethoxy)-2-methyl-benzene (1.40 g, 5.09 mmol) in Et2O (25 mL). The two-layered solution is stirred vigorously at ambient temperature under nitrogen for 2 days. Et2O (50 mL) and saturated aqueous NaCl solution (25 mL) are added to the mixture. The organic layer is separated, washed with a half-saturated aqueous NaCl solution (30 mL) containing saturated NaHCO3 (0.5 mL), dried over MgSO4, filtered and concentrated at ambient temperature to give 1.36 g of the crude (4-bromo-2-methyl-phenoxy)acetaldehyde as oil. The oil is diluted in Et2O to form a stock solution (67 mg/mL), which is used for the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414063B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-36d53961a31b4a5580efbc5935d2a03d |
| Source note | uspto-grants-2008_08 |