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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2269879Erstellt: 24. Oktober 2026

Methanesulfonyl chloride → 3,4,5-Trimethoxybenzyl Mesylate

https://huagongshe.com/de/reaction/2269879

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanesulfonyl chlorideHCID 31297—
Edukt3,4,5-Trimethoxybenzyl alcoholHCID 77449—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelAcetonitrileHCID 6342—
Produkt3,4,5-Trimethoxybenzyl MesylateHCID 18464591—

Reaktionsschritte

Combine 3,4,5-trimethoxy-benzyl alcohol (9.0 g, 45.4 mmol), diisopropylethylamine (12.9 g, 100 mmol), and acetonitrile (60 mL). Cool in an ice bath. Add methanesulfonyl chloride (6.76 , 49.0 mmol). After 2 hours, partition the reaction mixture between water and ethyl acetate. Separate the layers and extract the organic layer with 1 M hydrochloric acid solution and them a saturated solution of sodium bicarbonate. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06329392B1
Quelldatensatzuspto-grants-2001_12
ORD IDord-87018fd455e044e9a2f30a01c3ae272a
Quellennotizuspto-grants-2001_12