CID 406 → Diethyl 1-methoxy-1-(4-chloro-3-methoxyphenyl)methane phosphonate

온도

-78 °C

A solution of dimethyl acetal 3 (4.3 g, 20 mmol), sieve-dried CH2 Cl2 (20 ml) and triethyl phosphite (4.1 ml, 24 mmol) was stirred under argon at -78° C. Boron trifluoride ethereate (2.95 ml, 24 mmol) was added dropwise at -78° C., the solution was stirred 5 min and stored overnight at -20° C. The next day the reaction was warmed to room temperature and stirred 5 hours to complete phosphonate formation. With vigorous stirring, the reaction was quenched with solid NaHCO3 followed by 40 ml saturated NaHCO3 solution. After gas evolution ceased, 40 ml CH2Cl2 and 20 ml H2O were added, the biphasic mixture was partitioned and the CH2Cl2 phase was recovered, dried over Na2SO4 and evaporated. After pumping in vacuo, the oil was purified on a silica gel plug, eluting with CH2 Cl2 to yield phosphonate 4 as a light yellow oil (6.01 g., 99%).

1. stirringthe solution was stirred 5 min
2. temperatureThe next day the reaction was warmed to room temperature
3. stirringstirred 5 hours
4. customWith vigorous stirring, the reaction was quenched with solid NaHCO3
5. addition40 ml CH2Cl2 and 20 ml H2O were added
6. customthe biphasic mixture was partitioned
7. customthe CH2Cl2 phase was recovered
8. dry with materialdried over Na2SO4
9. customevaporated
10. customthe oil was purified on a silica gel plug
11. washeluting with CH2 Cl2

ORD 기록

ord-01aa363c17fa40d99d4ff945e622cef2

출처 데이터셋

uspto-grants-1998_11

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05840919