m-Chloroperbenzoic acid → 3-Chlorobenzoic Acid

A 500 mL three neck flask equipped with a stirrer, thermometer, condenser and 200 mL additional funnel was charged with 10 g (0.0151 mol) of Twin 9a and 100 mL of dichloromethane. The stirrer was started, and the temperature was lowered to 0° C. with an ice bath. 15.59 g (0.0904 mol) of MCPBA was dissolved in 150 mL of dichloromethane and added dropwise over a 30 minute period to the Twin 9a solution. The solution was allowed to warm to room temperature. Stirring continued for 12 hours at room temperature. During the reaction, a precipitate (3-chlorobenzoic acid) formed. The reaction mixture was filtered and the filtrate was washed with 500 mL of 5% sodium bisulfite to destroy residual peracid, and next with 500 mL of 2.5% sodium bicarbonate to extract 3-chlorobenzoic acid. Finally, it was washed with 500 mL of saturated aqueous sodium chloride and then dried over magnesium sulfite. The solvent was removed under reduced pressure to yield a pale yellow solid. The solid was recrystallized from 200 mL of 70/30 ethyl acetate/2-propanol to yield after vacuum drying 6.98 g of white crystals. 1HNMR (CDCl3, 23° C.): δ 8.1 (4H, d, aromatic), 6.9-7.1 (12H, m, aromatic), 4.3-4.4 (2H, d, CH glycidyl), 4.0-4.1 (2H, d, CH glycidyl), 3.9-4.0 (4H, m, CH2 octyl), 3.3-3.4 (2H, m, CH2 glycidyl), 2.9-3.0 (2H, t, CH glycidyl), 2.8 (2H, t, CH glycidyl), 1.7-1.9 (4H, m, CH2 octyl), 1.3-1.6 (8H, m, CH2 octyl).

1. customthe temperature was lowered to 0° C. with an ice bath
2. customDuring the reaction

ORD record

ord-2c77b0142654418f8686458dd0ed6a9d

Source dataset

uspto-grants-1998_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05811504