Hydrochloric Acid → HCID 22220991, compound

To a solution of diethyl malonate (10.1 g) in tetrahydrofuran (60 ml) was gradually added sodium hydride (60%, oil, 2.29 g) at 0° C. The mixture was stirred for 10 min and a solution of 4-chloromethyl-5-(5-chloro-2-thienyl)isoxazole (6.70 g) in tetrahydrofuran (60 ml) was added dropwise at 0° C. The mixture was stirred at room temperature for 15 hr. The reaction mixture was acidified by pouring into 2N hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was concentrated and the residue was dissolved in a mixture of 6N hydrochloric acid (80 ml) and acetic acid (120 ml). The mixture was heated under reflux for 8 hr. The reaction mixture was concentrated, and water was added to the residue. The obtained colorless crystals were filtrated, dried and recrystallized from ethyl acetate to give a colorless prism (4.95 g, yield 67%) of 3-[5-(5-chloro-2-thienyl)-4-isoxazolyl]propionic acid. melting point: 138–139° C.

1. customat 0° C
2. stirringThe mixture was stirred at room temperature for 15 hr
3. extractionextracted with ethyl acetate
4. concentrationThe ethyl acetate layer was concentrated
5. dissolutionthe residue was dissolved in a mixture of 6N hydrochloric acid (80 ml) and acetic acid (120 ml)
6. temperatureThe mixture was heated
7. temperatureunder reflux for 8 hr
8. concentrationThe reaction mixture was concentrated
9. additionwater was added to the residue
10. filtrationThe obtained colorless crystals were filtrated
11. customdried
12. customrecrystallized from ethyl acetate

ORD record

ord-30130b12aa934114b01275c6b60d1578

Source dataset

uspto-grants-2006_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US07022725B2