Dicyclohexylcarbodiimide → HCID 19936819, compound

A stirred solution of 711 mg (5.0 mmol) of 3-thienylacetic acid, 720 mg (5.0 mmol) of Meldrum's acid, and 610 mg (5.0 mmol) of 4-dimethylaminopyridine in 10 mL of DCM was treated with a solution of 1.03 g (5.0 mmol) of DCC in 10 mL of DCM. The resulting solution was stirred at room temperature for 16 h, during which time a white precipitate appeared in the reaction mixture. The reaction mixture was filtered through a pad of Celite to remove the precipitated dicyclohexylurea and the filtrate was washed successively with 1 N HCl (1×15 mL), H2O (1×15 mL), brine (1×15 mL). The filtrate was dried (MgSO4) and solvents were removed in vacuo. The resulting crude oil was dissolved in 8 mL of absolute ethanol and heated to 80° C. for 4 h. The reaction mixture was cooled to room temperature and ethanol was removed in vacuo. Purification of the resulting oil by silica gel flash column chromatography eluting with hexanes/EtOAc 2:1 afforded 1.02 g (97%) of the title compound as a yellow oil: 1H NMR (CDCl3, 400 MHz) δ 7.27 (m, 1H), 7.06 (s, 1H), 6.92 (m, 1H), 4.09 (q, 2H, J=6.8), 3.83 (s, 2H), 3.41 (s, 2H), 1.22 (t, 3H, J=6.8).

1. filtrationThe reaction mixture was filtered through a pad of Celite
2. customto remove the precipitated dicyclohexylurea
3. washthe filtrate was washed successively with 1 N HCl (1×15 mL), H2O (1×15 mL), brine (1×15 mL)
4. dry with materialThe filtrate was dried (MgSO4) and solvents
5. customwere removed in vacuo
6. dissolutionThe resulting crude oil was dissolved in 8 mL of absolute ethanol
7. temperatureheated to 80° C. for 4 h
8. temperatureThe reaction mixture was cooled to room temperature
9. customethanol was removed in vacuo
10. customPurification of the resulting oil by silica gel flash column chromatography
11. washeluting with hexanes/EtOAc 2:1

ORD record

ord-b7af59a956d44ff5a82c15a707c56814

Source dataset

uspto-grants-2007_03

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07189851B2