تفاعل #708771
ord-c8ca4b935cf346f784b0bc78f3982d0a
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1درجة الحرارةto cool
- 2استخلاصThe reaction mixture was extracted with diethyl ether (3×120 ml)
- 3غسيلthe combined ether extracts washed with saturated brine
- 4تجفيفdried (MgSO4)
- 5أخرىevaporated
- 6workup.DISSOLUTIONThe residue was dissolved
- 7workup.STIRRINGstirred in tetrahydrofuran (30 ml)
- 8workup.WAIT3M hydrochloric acid (30 ml) for 2 hours
- 9workup.ADDITIONThe mixture was diluted with water (100 ml)
- 10استخلاصextracted with diethyl ether (300 ml)
- 11غسيلThe ether was washed with saturated sodium hydrogen carbonate solution (2×50 ml) and saturated brine
- 12تجفيفdried (MgSO4)
- 13أخرىevaporated
- 14أخرىThe residue was purified by flash column chromatography on silica
- 15غسيلeluting with n-hexane/ethyl acetate (80:20:, by volume)
الإجراء التجريبي
A solution of lithium (77 mg) in methanol (30 ml) was added during 2 hours to a stirred suspension of 2-cyanobenzaldehyde and (1,3-dioxolan-2-yl-methyl)-triphenyl phosphonium bromide (4.71 g) in dimethylformamide (34 ml) at 85° C. The mixture was stirred at 85° C. for 6 hours, allowed to cool and poured into water (450 ml). The reaction mixture was extracted with diethyl ether (3×120 ml) and the combined ether extracts washed with saturated brine, dried (MgSO4) and evaporated. The residue was dissolved and stirred in tetrahydrofuran (30 ml) and 3M hydrochloric acid (30 ml) for 2 hours. The mixture was diluted with water (100 ml) and extracted with diethyl ether (300 ml). The ether was washed with saturated sodium hydrogen carbonate solution (2×50 ml) and saturated brine, dried (MgSO4) and evaporated. The residue was purified by flash column chromatography on silica, eluting with n-hexane/ethyl acetate (80:20:, by volume) to give as a pale yellow solid 2-cyano-(E)-cinnamaldehyde (504 mg, 45%) m.p. 107°-110° C.; NMR: 6.82 (1H, q), 7.69 (5H, m) and 9.81 (1H, d); m/e 157 (M+).