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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1737450Erstellt: 26. Oktober 2026

N-Methylphenylethanolamine → HCID 21842621, Verbindung

https://huagongshe.com/reaction/1737450

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylphenylethanolamineHCID 913—
EduktBenzenesulfonyl chlorideHCID 7369—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 21842621HCID 21842621—

Reaktionsschritte

A solution of α-(methylaminomethyl)benzyl alcohol (1.00 g, 6.61 mmol) in 15 mL of THF was cooled in an ice bath. Benzenesulfonyl chloride (0.886 mL, 1.23 g, 6.94 mmol) and N,N-diisopropylethylamine (2.3 mL, 1.7 g, 13 mmol) were added and mixture was allowed to warm to room temperature. After 30 min, the solvent was evaporated and the residue was partitioned between 50 mL of ethyl acetate and 40 mL of saturated aqueous sodium bicarbonate. The aqueous layer was extracted with 2×50 mL of ethyl acetate. The combined organic layers were washed with 50 mL of brine, dried over sodium sulfate, and evaporated. Purification by flash column chromatography on silica gel, eluting with 20-50% ethyl acetate in hexane, gave the title compound in quantitative yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05962462
Quelldatensatzuspto-grants-1999_10
ORD IDord-ba598985bff041bf90162b74bd66b628
Quellennotizuspto-grants-1999_10