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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1096822Erstellt: 26. Oktober 2026

Methanol → Benzenemethanol, 3,5-dichloro-4-hydroxy-

https://huagongshe.com/reaction/1096822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktWaterHCID 962—
Edukt3,5-Dichloro-4-hydroxybenzoic acidHCID 18749—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzenemethanol, 3,5-dichloro-4-hydroxy-HCID 176409—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

BH3 (1M in THF, 250 mL, 250 mmol) was added dropwise to a cooled sol. of 3,5-dichloro-4-hydroxybenzoic acid (20 g, 96.6 mmol) in THF (200 mL) at 0° C. The resulting mixture was stirred at 0° C. for 15 min., and then at rt for 13 h. The milky mixture was cooled to 0° C., and MeOH (150 mL), then water (100 mL), were added dropwise. The mixture was further stirred at 0° C. for 15 min, and then at rt for 5 h. The mixture was then partially concentrated under reduced pressure. EtOAc (200 mL) and water (50 mL) were added to the residue, and the phases were shaken and separated. The aq. phase was further extracted with EtOAc. The combined org. extracts were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by FC(CH2Cl2/CH3OH, 100:1) led to the title compound as a slightly beige solid (17.86 g, 96%). LC-MS: tR=0.69 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08138340B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-90e996b781944c7a9eb2dd649fbe0bcb
Quellennotizuspto-grants-2012_03