HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 424800Erstellt: 24. Oktober 2026
4-Iodo-3-methylbenzoic acid → (4-Iodo-3-methylphenyl)methanol
https://huagongshe.com/de/reaction/424800
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Iodo-3-methylbenzoic acid | HCID 1517322 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (4-Iodo-3-methylphenyl)methanol | HCID 53843601 | 95% |
Reaktionsschritte
To a solution of 4-iodo-3-methyl-benzoic acid (5.2 g, 20 mmol) in THF (30 mL), is added 2.0 M borane-dimethyl sulfide complex in THF (40.0 mL, 80 mmol) dropwise. The reaction mixture is stirred overnight. The reaction mixture is quenched carefully at 0° C. with methanol (20 mL) and the mixture is evaporated to dryness under reduced pressure. The residue is partitioned between EtOAc (80 mL) and water (60 mL). The organic phase is washed with brine (60 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure to a residue. The residue is purified by flash chromatography (AnaLogix, gradient EtOAc/Hexane) to give (4-Iodo-3-methyl-phenyl)-methanol as white solid (4.7 g, 95%). 1HNMR (CDCl3) (ppm): 2.4 (3H, s), 4.55 (2H, s), 6.8-7.75 (3H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08106077B2 |
|---|
| Quelldatensatz | uspto-grants-2012_01 |
|---|
| ORD ID | ord-c972eae0d6c14fa291d1d2d6dbb11997 |
|---|
| Quellennotiz | uspto-grants-2012_01 |
|---|