Hydrogen Bromide → 2-Bromo-1-(2,4-dimethyl-1,3-thiazol-5-yl)ethan-1-one

N,N,N-Trimethylanilinium bromide-bromine (1:1:1) (1.84 g, 4.9 mmol) was added to a solution of 1-(2,4-dimethyl-1,3-thiazol-5-yl)ethanone (800 mg, 5.15 mmol) in diethyl ether (9 mL) and acetonitrile (3 mL), and HBr in acetic acid (33% w/w, 4 mL). The mixture was stirred for 1 h. The reaction mixture was diluted with diethyl ether (25 mL) and washed with aqueous Na2S2O5 solution (5% w/v, 20 mL). The organic phase was separated off, and the aqueous phase was extracted with diethyl ether (25 mL). The organic phases were combined, then washed with saturated aqueous NaHCO3 solution (2×25 mL) and brine. The residue was dried over sodium sulfate, then filtered and concentrated under vacuum, to give the title compound (764 mg, 63%) as a light brown oil. δH (250 MHz, CDCl3) 4.22 (s, 2H), 2.69-2.76 (br s, 6H).

1. washwashed with aqueous Na2S2O5 solution (5% w/v, 20 mL)
2. customThe organic phase was separated off
3. extractionthe aqueous phase was extracted with diethyl ether (25 mL)
4. washwashed with saturated aqueous NaHCO3 solution (2×25 mL) and brine
5. dry with materialThe residue was dried over sodium sulfate
6. filtrationfiltered
7. concentrationconcentrated under vacuum

ORD-Eintrag

ord-a6d3c96e863f4c1085269db57404e619

Quelldatensatz

uspto-grants-2016_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US09309243B2