3-Methylthiophene → Thiophene, 4-methyl-2-[4-(trifluoromethyl)phenyl]-

温度

0 °C

To a solution of 3-methylthiophene (2.31 ml) in anhydrous THF (75 ml) at −78° C. under N2 was added dropwise n-BuLi (1.6 M in hexanes, 15 ml). Thirty minutes after the addition was complete, the reaction mixture was allowed to warm to 0° C. and stirred for a further 30 minutes. Zinc chloride (0.5 M in THF, 48 ml) was added drop-wise, after a further 15 minutes palladium (0) tetrakis(triphenylphosphine) (100 mg) and 4-bromobenzotrifluoride (3.36 ml) were added and the reaction allowed to attain room temperature. The reaction mixture was warmed to 40° C. and stirred at this temperature for 3 hours. The reaction mixture was then cooled to room temperature and the solvents removed in vacuo. The residue was partitioned between and ether and the aqueous extract further washed with ether. The combined organic extracts were dried (MgSO4), filtered and evaporated to yield a brown oil. Purification by Biotage® chromatography eluting with cyclohexane yielded the title compound as a white solid.

1. additionThirty minutes after the addition
2. customto attain room temperature
3. temperatureThe reaction mixture was warmed to 40° C.
4. stirringstirred at this temperature for 3 hours
5. temperatureThe reaction mixture was then cooled to room temperature
6. customthe solvents removed in vacuo
7. customThe residue was partitioned between and ether
8. extractionthe aqueous extract further
9. washwashed with ether
10. dry with materialThe combined organic extracts were dried (MgSO4)
11. filtrationfiltered
12. customevaporated
13. customto yield a brown oil
14. customPurification by Biotage® chromatography
15. washeluting with cyclohexane

ORDレコード

ord-15ae2bc802194632a49a178c7691a128

出典データセット

uspto-grants-2006_08

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07091237B2