Acetone → 5-Thiazolemethanol, 2-amino--alpha-,-alpha--dimethyl-

온도

-78 °C

To a −78° C. solution of thiazol-2-amine (7.0 g, 69.9 mmol) in tetrahydrofuran (200 ml) was added a 10.0 M solution of butyllithium in hexane (14 mL, 140 mmol). The mixture was stirred at −78° C. for 1 hour and chlorotrimethylsilane (15.2 g, 140 mmol) was added dropwise. The mixture was allowed to warm up to −40° C., cooled to −78° C. and a 10.0 M solution of butyllithium in hexane (7.0, 70 mmol) was added After 10 minutes, propan-2-one (8.12 g, 140 mmol) was added and the mixture was stirred for 12 hours. The reaction mixture was quenched with saturated aqueous NH4Cl and extracted with ether. The organic extract was dried (Na2SO4), filtered and concentrated. The residue was purified by column chromatography using an Analogix® Intelliflash280™ (SiO2, 0-100% ethyl acetate in hexanes) to afford the title compound. 1H NMR (500 MHz, CDCl3) δ ppm 1.61 (s, 6H) 5.04-5.19 (brs, 2H) 6.89 (s, 1H); MS (ESI) m/z 159 (M+H)+.

1. temperatureto warm up to −40° C.
2. temperaturecooled to −78° C.
3. stirringthe mixture was stirred for 12 hours
4. customThe reaction mixture was quenched with saturated aqueous NH4Cl
5. extractionextracted with ether
6. extractionThe organic extract
7. dry with materialwas dried (Na2SO4)
8. filtrationfiltered
9. concentrationconcentrated
10. customThe residue was purified by column chromatography

ORD 기록

ord-1220d8aab49a43c5aa54d6b23677f4df

출처 데이터셋

uspto-grants-2013_10

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08546583B2