tert-Butyl peroxybenzoate → 3-Bromo-2-t-butoxythiophene

A -78° C. solution of 2,3-dibromothiophene (Aldrich, 10.0 g, 41.3 mmol) in 150 mL of diethyl ether was treated with n-butyl lithium (2.5 M, 16.5 mL) over a 20 min period. The mixture was stirred 1h at -78° C. Magnesium bromide (13.0 g, 49.6 mmol) was added as a solid in two portions. The mixture was stirred at -780° C. for 1h and rt for 2h. t-Butylperbenzoate was added at 0° C. and the reaction was allowed to stir at ambient temperature overnight. The mixture was quenched with ice water (50 mL) and 2N HCl (25 mi). The organic layer was separated and washed once with ice cold 1 N NAOH, water and brine. The organic layer was dried over magnesium sulfate and concentrated to give 10.5 g (98%) of the title compound: MS: m/z 236 MH+); 1H NMR(CDCl3): d 1.36 (s, 9H), 6.61 (d, j=6.1 Hz, 1H) and 7.23 (d, J=6.1 Hz, 1H).

1. additionwas added at 0° C.
2. customThe mixture was quenched with ice water (50 mL) and 2N HCl (25 mi)
3. customThe organic layer was separated
4. washwashed once with ice cold 1 N NAOH, water and brine
5. dry with materialThe organic layer was dried over magnesium sulfate
6. concentrationconcentrated

ORD record

ord-7e57dc7d317a4c2aad970193a1e0d4ad

Source dataset

uspto-grants-1994_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05284857