Chloroacetone → HCID 12708701、化合物

温度

120 °C

Cinnamamide (2.0 g, 14 mmol), chloroacetone (0.93 mL, 16 mmol), and K2CO3 (940 mg, 6.8 mmol) were combined under argon and the mixture was heated in a 120° C. oil bath. The reaction mixture solidified and stirring stopped upon heating. After 16 h, the cooled reaction mixture was quenched by the addition of water (20 mL) and then diluted with ethyl acetate (100 mL). The organic phase was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography eluting with 90:10 hexane:ethyl acetate. The product that was obtained (280 mg) showed some close running impurities by thin layer chromatography (TLC). The material was further purified by preparative TLC via multiple elutions with 95:5 hexane:ethyl acetate. Isolation of the middle of the main band afforded 4-methyl-2-[(E)-2-phenylethenyl]-1,3-oxazole (47.0 mg, 2% yield) as a yellow oil. 1H NMR (CDCl3, 300 MHz) δ 7.53-7.32 (m, 7H), 6.91 (d, J=16.4 Hz, 1H), 2.21 (s, 3H). MS (ESI) 185.7 (M++H).

1. temperatureupon heating
2. customthe cooled reaction mixture
3. customwas quenched by the addition of water (20 mL)
4. additiondiluted with ethyl acetate (100 mL)
5. dry with materialThe organic phase was dried over Na2SO4
6. filtrationfiltered
7. concentrationconcentrated in vacuo
8. customThe crude product was purified by column chromatography
9. washeluting with 90:10 hexane
10. customThe product that was obtained (280 mg)
11. customThe material was further purified by preparative TLC via multiple elutions with 95:5 hexane

ORDレコード

ord-4f70dc254882405b8c8f758a8eba7b3c

出典データセット

uspto-grants-2005_10

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06956049B1