Hydrochloric Acid → 5-Bromo-2-chloro-1-methyl-3-(2,2,2-trichloro-ethyl)-benzene

CuCl2 (8.0 g, 0.06 mol) and tert-butylnitrile (8.9 mL, 0.074 mol) are suspended in acetonitrile (60 mL). 1,1-dichloroethylene is added dropwise at 20° C. 5-Bromo2-chloro-3-methyl-phenylamine (11.0 g, 0.05 mol), dissolved in acetonitrile (60 mL), is added and the reaction is stirred at RT for 3 h. The mixture is poured into aqueous 20% HCl (150 mL) and the aqueous phase is extracted with CH2Cl2 (2×150 mL). The organic phase is dried over Na2SO4 and the solvent is evaporated. The residue is purified by FCC (hexane/CH2Cl2 9:1) to afford 5-bromo-2-chloro-1-methyl-3-(2,2,2-trichloro-ethyl)-benzene. The intermediate is redissolved in MeOH (80 mL) and heated to 70° C. A solution of 5.4 M NaOMe in MeOH (28.4 mL) is added dropwise and the reaction is stirred at 70° C. for 3 h. The reaction is cooled to RT and concentrated H2SO4 (10 mL) is added. The reaction is stirred at reflux for 1 h. The mixture is diluted with H2O (200 mL) and extracted with CH2Cl2 (2×200 mL). The combined organic phases are dried over Na2SO4 and the solvent is evaporated. The residue is purified by FCC (hexane/CH2Cl2 9:1 to 1:1) to afford (5bromo-2-chloro-3-methyl-phenyl)-acetic acid methyl ester. 1H NMR (CDCl3, 400 MHz) δ 2.26 (s, 3H), 3.61 (s, 3H), 3.63 (s, 2H), 7.15 (s, 1H), 7.21 (s, 1H).

1. additionis added
2. extractionthe aqueous phase is extracted with CH2Cl2 (2×150 mL)
3. dry with materialThe organic phase is dried over Na2SO4
4. customthe solvent is evaporated
5. customThe residue is purified by FCC (hexane/CH2Cl2 9:1)

ORD record

ord-93914cd6a283471cb2b6d0a133bd8be1

Source dataset

uspto-grants-2008_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07358253B2