تفاعل #41132
ord-f162d2aee57f4371ba5eb6e5a8135f3d
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةmaintaining internal temperature below 5° C
- 2درجة الحرارةto warm up to room temp.
- 3workup.STIRRINGto stir at room temp. for 18 h
- 4تركيزThe reaction mixture was concentrated in vacuo and 1 L of solvent
- 5أخرىwas removed
- 6درجة الحرارةThe remaining brownish solution with white solid in it was cooled in an ice-bath
- 7workup.ADDITIONhydrochloric acid (6N, 200 ml) was added
- 8درجة الحرارةmaintaining internal temperature below 20° C
- 9درجة الحرارةThe resulting bright yellow suspension was then warmed up to room temp.
- 10workup.STIRRINGstirred for 1 h
- 11أخرىAdditional 700 ml solvent was removed in vacuo at room temp
- 12workup.ADDITIONWater (400 ml) was added
- 13workup.DISSOLUTIONto dissolve all the white solid and ethyl acetate (500 ml)
- 14workup.ADDITIONwas added
- 15أخرىthe mixture transferred to a separatory funnel
- 16استخلاصThe aqueous was extracted once with ethyl acetate (200 ml)
- 17غسيلThe combined organic extracts was washed once with brine (100 ml)
- 18تجفيفAfter drying over MgSO4
- 19تركيزconcentrating in vacuo
الإجراء التجريبي
Ethyl 3,3-diethoxypropionate (100 g, 525.7 mmol) was dissolved in THF (360 ml) at room temp. Ethyl formate (175.1 ml, 2.1 mol) was added at room temp. The solution was cooled in an ice-bath to 0° C. and tBuOK (1M solution in THF, 1,156 ml, 1.156 mol) was added via an addition funnel slowly over 30 min, maintaining internal temperature below 5° C. The color changed instantly from colorless to dark orange. The reaction mixture was allowed to warm up to room temp. and stirred for 2 h. The reaction was allowed to stir at room temp. for 18 h. The reaction mixture was concentrated in vacuo and 1 L of solvent was removed. The remaining brownish solution with white solid in it was cooled in an ice-bath and hydrochloric acid (6N, 200 ml) was added to adjust pH=3, maintaining internal temperature below 20° C. The resulting bright yellow suspension was then warmed up to room temp. and stirred for 1 h. Additional 700 ml solvent was removed in vacuo at room temp. Water (400 ml) was added to dissolve all the white solid and ethyl acetate (500 ml) was added and the mixture transferred to a separatory funnel. The aqueous was extracted once with ethyl acetate (200 ml). The combined organic extracts was washed once with brine (100 ml). After drying over MgSO4 and concentrating in vacuo, 2-formyl-3-oxo-propionic acid ethyl ester (75.85 g) was obtained as yellow oil.