تفاعل #3775
ord-58615e62df594250977665f017188dc0
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONto minimize mixing
- 2أخرىSeal the pressure vessel
- 3workup.ADDITION(Caution, upon mixing a sharp rise in pressure
- 4استخلاصExtract repeatedly with ethyl acetate
- 5استخلاصextract repeatedly with aqueous 10% potassium bicarbonate solution
- 6درجة الحرارةcool in an ice-bath
- 7استخلاصExtract the acidified aqueous layer repeatedly with ethyl acetate
- 8استخلاصextract with saturated aqueous sodium chloride solution
- 9تجفيفdry over MgSO4
- 10ترشيحfilter
- 11أخرىevaporate in vacuo
الإجراء التجريبي
Combine (S)-7-[(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)]-1,2,6,7,8,12b-hexahydro-6-oxopyrido[2,1-a][2]benzazepine (800 mg, 2.2 mmol) and sulfuric acid (24 mL) in a pressure vessel. Carefully, add formic acid (4.0 mL, 87 mmol) to minimize mixing and thereby the formation of carbon monoxide. Seal the pressure vessel and add carbon monoxide to 300 psi before stirring. (Caution, upon mixing a sharp rise in pressure will occur.) After 16 hours, vent the vessel and add the reaction mixture to an ice/water mixture (160 mL). Extract repeatedly with ethyl acetate. Combine the organic layers and extract repeatedly with aqueous 10% potassium bicarbonate solution. Combine the potassium bicarbonate solution layers and cool in an ice-bath. Acidify to pH 1 using aqueous 6M hydrochloric acid solution. Extract the acidified aqueous layer repeatedly with ethyl acetate. Combine the organic layers and extract with saturated aqueous sodium chloride solution, dry over MgSO4, filter, and evaporate in vacuo to give the title compound.