Toluene → 2-(2-Chloro-4-(trifluoromethyl)pyrimidin-5-yl)propan-2-ol

Temperature

-78 °C

To a 1.0 M solution of TiCl4 in toluene (6.67 mL, 6.67 mmol) was added a 1.6 M solution of MeLi in Et2O (4.18 mL, 6.69 mmol) dropwise a −78° C. (dry ice/acetone bath). The resulting dark solution stirred at −78° C. for 30 minutes. A solution of 1-(2-chloro-4-(trifluoromethyl)pyrimidin-5-yl)ethanone (500 mg, 2.23 mmol) in Et2O (3 mL) was added dropwise at −78° C. The reaction was slowly allowed to warm to rt in the dewar over a 15 h period. TLC analysis showed complete conversion to the more polar tertiary alcohol product. The mixture was then cooled to 0° C. and quenched with sat. aq. NH4Cl (10 mL) followed by EtOAc (10 mL) for the workup. The EtOAc layer was separated and the aqueous layer was extracted with EtOAc (2×10 mL). The EtOAc layers were combined, dried using Na2SO4 and evaporated to give the crude product. Purification using ISCO FCC eluting with 20% EtOAc in Hexanes gave 459 mg of 2-(2-chloro-4-(trifluoromethyl)pyrimidin-5-yl)propan-2-ol (86% yield) as a colorless oil. LC-MS MS (ESI) m/z 241.12 [M+H]+. 1H NMR (CDCl3, 400 MHz): δ 9.05 (s, 1H), 1.99 (s, 1H), 1.67 (s, 6H).

1. temperatureto warm to rt in the dewar over a 15 h period
2. temperatureThe mixture was then cooled to 0° C.
3. customquenched with sat. aq. NH4Cl (10 mL)
4. customThe EtOAc layer was separated
5. extractionthe aqueous layer was extracted with EtOAc (2×10 mL)
6. customdried
7. customevaporated
8. customto give the crude product
9. customPurification
10. washeluting with 20% EtOAc in Hexanes

ORD record

ord-0fdfe097fa2b4dba8dfe1626fdc39bbb

Source dataset

uspto-grants-2016_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09416135B2