تفاعل #708771

ord-c8ca4b935cf346f784b0bc78f3982d0a

معادلة التفاعل

O
water
[Li]
lithium
N#Cc1ccccc1C=O
2-cyanobenzaldehyde
[Br-].c1ccc([P+](CC2OCCO2)(c2ccccc2)c2ccccc2)cc1
(1,3-dioxolan-2-yl-methyl)-triphenyl phosphonium bromide
N#Cc1ccccc1/C=C/C=O
2-cyano-(E)-cinnamaldehyde
المردود 45.0%

ظروف التفاعل

درجة الحرارة
85°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto cool
  2. 2
    استخلاصThe reaction mixture was extracted with diethyl ether (3×120 ml)
  3. 3
    غسيلthe combined ether extracts washed with saturated brine
  4. 4
    تجفيفdried (MgSO4)
  5. 5
    أخرىevaporated
  6. 6
    workup.DISSOLUTIONThe residue was dissolved
  7. 7
    workup.STIRRINGstirred in tetrahydrofuran (30 ml)
  8. 8
    workup.WAIT3M hydrochloric acid (30 ml) for 2 hours
  9. 9
    workup.ADDITIONThe mixture was diluted with water (100 ml)
  10. 10
    استخلاصextracted with diethyl ether (300 ml)
  11. 11
    غسيلThe ether was washed with saturated sodium hydrogen carbonate solution (2×50 ml) and saturated brine
  12. 12
    تجفيفdried (MgSO4)
  13. 13
    أخرىevaporated
  14. 14
    أخرىThe residue was purified by flash column chromatography on silica
  15. 15
    غسيلeluting 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+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04824858uspto-grants-1989_04