Chloride → 1-(2,3,6-Trifluorophenyl)propan-2-one

温度

40 °C

A mixture of CeCl3 (438 g, 1779 mmol) and THF (12 L) was heated at 40° C. for about 2 h then cooled to 5° C. Methylmagensium chloride in THF (3 M, 3.4 L) was charged at 5-9° C. and then it was warmed up to 16° C. and held for 1 h. The suspension was re-cooled to −10 to −15° C. A solution of 17 (1.19 kg) in THF (2.4 L) was charged into the suspension over 15 min. After confirmation of completion of the reaction, the reaction mixture was transferred to a cold solution of hydrochloric acid (2 N, 8.4 L) and MTBE (5 L) in 5-10° C. The aqueous phase was separated and the organic layer was washed with aqueous 5% K2CO3 (6 L) and then 10% aqueous NaCl (5 L). The organic layer was dried over Na2SO4, concentrated to give crude 18 (917 g, >99 wt %) in 95% yield. The crude 18 was used in the next step without further purification. Analytically pure 18 was obtained by silica gel column.

1. temperaturethen cooled to 5° C
2. temperatureit was warmed up to 16° C.
3. temperatureThe suspension was re-cooled to −10 to −15° C
4. customAfter confirmation of completion of the reaction
5. customThe aqueous phase was separated
6. washthe organic layer was washed with aqueous 5% K2CO3 (6 L)
7. dry with materialThe organic layer was dried over Na2SO4
8. concentrationconcentrated
9. customto give crude 18 (917 g, >99 wt %) in 95% yield
10. customThe crude 18 was used in the next step without further purification
11. customAnalytically pure 18 was obtained by silica gel column

ORDレコード

ord-12bb6af8d848469db0d130bc4014a607

出典データセット

uspto-grants-2015_11

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US09174989B2