HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (3-Bromo-5-iodophenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 3-bromo-5-iodobenzoate | HCID 21942573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-Bromo-5-iodophenyl)methanol | HCID 15467379 | 96.7% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To methyl 5-bromo-3-iodobenzoate (Step A above) (5.01 g, 0.015 mole) in anhydrous methylene chloride (100 mL) at -78° C., was added dropwise minutes, diisobutylaluminum hydride (5.50 mL, 0.03 mole). The mixture was stirred for 1 hour then allowed to warm to 0° C. The reaction solution was poured into 600 mL, chilled 3N HCl and extracted 3× with methylene chloride (150 mL). The organic layers were combined, dried over MgSO4 and concentrated under vacuum to yield 5-bromo-3-iodobenzyl alcohol (4.54 g) as a white solid. MP=110-112° C. MS and NMR were consistent with the desired structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06028223 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-7a3136ee0bb84c16864a250cede4929f |
| Source note | uspto-grants-2000_02 |