HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 4-Bromo-1-chloro-2-isopropoxybenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-Bromo-2-chlorophenol | HCID 820392 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-1-chloro-2-isopropoxybenzene | HCID 21071029 | — |
Reaction Steps
To 1.70 g (6.5 mmol) of triphenylphosphine in 25 mL of CH2Cl2 at 0° C. was added 1.14 g (6.5 mmol) of diethylazodicarboxylate. After 10 minutes, 390 mg (6.5 mmol) of isopropanol was added, followed rapidly by 1.03 g (5.0 mmol) of 3-Bromo-6-chlorophenol. The reaction was complete within three hours, and was partitioned between ether and water. The phases were separated, and the ether phase was diluted with hexanes and washed twice with 10% aqueous methanol and once with brine. The ether/hexanes phase was dried over Na2SO4, filtered, and concentrated in vacuo to yield product as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157464B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-16a63f95237944259f1161f75fda48cd |
| Source note | uspto-grants-2007_01 |