Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 83876Erstellt: 23. Oktober 2026

Triethylamine → 3-Bromo-4-fluorobenzyl methanesulfonate

https://huagongshe.com/de/reaction/83876

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt3-Bromo-4-fluorobenzyl AlcoholHCID 2773351—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Bromo-4-fluorobenzyl methanesulfonateHCID 5985481382,1%

Reaktionsschritte

To a solution of (3-bromo-4-fluorophenyl)methanol (53 g, 0.258 mol) in DCM (500 mL) at 0° C. was added Et3N (108 mL, 775 mmol, 3 eq) and methanesulfonyl chloride (24 mL, 310 mmol, 1.2 eq) successively. After stirring 30 min, the reaction mixture was partitioned in DCM and water. The organic layer was dried over MgSO4 and evaporated in vacuo to give 3-bromo-4-fluorobenzyl methanesulfonate (60 g), which used to the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 7.65-7.62 (m, 1H), 7.37-7.33 (m, 1H), 7.16 (t, J=4.4 Hz, 1H), 5.17 (s, 2H), 2.99 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846739B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-ec7499c6f61a4e40a8ae183568bf4d73
Quellennotizuspto-grants-2014_09