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HRID 1264539Erstellt: 24. Oktober 2026

2,4,6-Trimethylpyridine → Methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl ester

https://huagongshe.com/de/reaction/1264539

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,4,6-TrimethylpyridineHCID 7953—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt2-[2-(Hydroxymethyl)phenyl]ethanolHCID 239024—
EduktLithium ChlorideHCID 433294—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl esterHCID 5432882645%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Mix 2-(2-hydroxymethyl-phenyl)-ethanol (12.0 g, 78.8 mmol) and collidine (23 mL, 0.17 mol) and treat with lithium chloride (7.35 g, 0.173 mmol) in dimethylformamide (125 mL). Cool in an ice bath and treat, by dropwise addition, with mesyl chloride (13.4 mL). Stir at 0° C. for 4 hours, partition between ice water (300 mL) and a 1:1 mixture of ether:pentane (2×400 mL). Wash the organic layer with a saturated solution of CuSO4 (2×200 mL), dry (MgSO4) and purify by silica gel chromatography (2.5:1 hexane/ethyl acetate followed by 2:1 hexane/ethyl acetate followed by 3:2 hexane/ethyl acetate) to give methanesulfonic acid 2-(2-chloromethyl-phenyl)-ethyl ester as a pale yellow oil (8.8 g, 45%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06544980B2
Quelldatensatzuspto-grants-2003_04
ORD IDord-acf7392e4e924400b8265eaf73daafc3
Quellennotizuspto-grants-2003_04