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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1096824Erstellt: 26. Oktober 2026

Water → (Rac.)-2,6-dichloro-4-(1-hydroxyethyl)phenol

https://huagongshe.com/reaction/1096824

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktAmmonium ChlorideHCID 25517—
EduktBenzenemethanol, 3,5-dichloro-4-hydroxy-HCID 176409—
EduktHCID 178418689HCID 178418689—
LösungsmittelDiethyl EtherHCID 3283—
Produkt(Rac.)-2,6-dichloro-4-(1-hydroxyethyl)phenolHCID 6678370395%

Reaktionsschritte

A sol. of 2,6-dichloro-4-hydroxymethylphenol (1.635 g, 8.56 mmol) in Et2O (30 mL) was cooled to −78° C. MeMgBr (3M in Et2O, 7.15 mL, 21.5 mmol) was added dropwise to the cooled reaction mixture over 18 min. Et2O (20 mL) was added again during the addition of MeMgBr. Stirring was continued at −78° C. for 1 h, and then the reaction mixture was allowed to warm up to rt over 1 h. The mixture was cooled to 0° C., and aq. sat. NH4Cl (10 mL) was added dropwise. The mixture was allowed to warm up to rt, and additional aq. sat. NH4Cl (35 mL) and water (35 mL) were added. The phases were then separated and the aq. phase was extracted with Et2O. The combined org. extracts were then washed with brine (50 mL), dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by FC (EtOAc/heptane, 1:1) yielded the title compound (1.683 g, 95%). LC-MS: tR=0.74 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08138340B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-1323216e7190463894eccacb68d735f7
Quellennotizuspto-grants-2012_03