Diisopropylamine → alpha-(4-Benzyloxyphenyl)-alpha-hydroxy-N,N-dimethyl-thioacetamide

온도

-78 °C

To a solution of distilled diisopropylamine (22.9 mL, 175 mmol) in 400 mL of anhydrous THF at −78° C. was added 1.6 M n-butyllithium in hexanes (100 mL, 160 mmol) over a period of 45 min. The mixture was stirred at −78° C. for 1.5 h. To the solution was cannulated over a period of 1 h a solution of 4-benzyloxybenzaldehyde (30.9 g, 146 mmol) and N,N-dimethylthioformamide (13.7 mL, 160 mmol) in 100 mL of distilled THF. The reaction mixture was stirred at −78° C. for 16 h. The reaction was then quenched with 500 mL of saturated NH4Cl solution. The mixture was extracted with EtOAc (3×1 L), and the combined organic layers were dried over MgSO4 and concentrated under reduced pressure. The residue was then recrystallyzed from EtOAc/hexanes to afford 20.0 g (66.5 mmol, 46%) of an off-white solid.

1. waitTo the solution was cannulated over a period of 1 h
2. stirringThe reaction mixture was stirred at −78° C. for 16 h
3. customThe reaction was then quenched with 500 mL of saturated NH4Cl solution
4. extractionThe mixture was extracted with EtOAc (3×1 L)
5. dry with materialthe combined organic layers were dried over MgSO4
6. concentrationconcentrated under reduced pressure

ORD 기록

ord-652d0d4055cd475da59033d9071b4c54

출처 데이터셋

uspto-grants-2001_08

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US06271227B1