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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132374Erstellt: 25. Oktober 2026

Pivaloyl chloride → N-(2-Bromo-5-fluorophenyl)pivalamide

https://huagongshe.com/reaction/132374

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPivaloyl chlorideHCID 62493—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Bromo-5-fluoroanilineHCID 2773317—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(2-Bromo-5-fluorophenyl)pivalamideHCID 59731998—

Reaktionsschritte

Trimethylacetyl chloride (4.2 mL, 34.1 mL) was fast dropwise added to a solution of 2-bromo-5-fluorobenzenamine (4.31 g, 22.7 mmol) in CH2Cl2 (50 mL) at room temperature, followed by the addition of DIEA (7.9 mL, 45.4 mmol). The resulting mixture was stirred at room temperature for 2 hrs, and then partitioned between HCl (1N, 200 mL) and EtOAc(250 mL). After separation, the organic phase was washed with brine (50 mL), dried on MgSO4, concentrated on rotary vacuum, and purified on flash chromatography eluting with 20˜40% EtOAc/hexanes (1200 mL) to afford the expected product, as a colorless oil (6.07 g, 98% yield); 1H NMR (400 MHz, CDCl3) δ ppm 1.33 (s, 9 H), 6.69 (ddd, J=8.81, 7.55, 3.02 Hz, 1 H), 7.45 (dd, J=8.81, 5.79 Hz, 1 H), 8.04 (s, 1 H), 8.28 (dd, J=11.08, 3.02 Hz, 1 H); Mass spec. 274.04 (MH+), Calc. for C11H13BrFNO 273.02.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384931B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-6eac0cac0b2943239349a0e0f20aabed
Quellennotizuspto-grants-2008_06