Hydrochloric Acid → 3-Perylenecarboxaldehyde

HRID 371304

反応式

HRID 371304 の反応式
N#N.[CH:3]1[C:20]2=[C:21]3[C:10]([C:11]4[C:22]5[C:15](=[CH:16][CH:17]=[CH:18][C:19]2=5)[CH:14]=[CH:13][CH:12]=4)=[CH:9][CH:8]=[CH:7][C:6]3=[CH:5][CH:4]=1.Cl[Sn](Cl)(Cl)Cl.ClC[CH:30]([O:33]C(CCl)CCl)CCl.Cl>O.ClC1C=CC=CC=1Cl>[CH:18]1[C:19]2=[C:22]3[C:11]([C:10]4[C:21]5[C:6](=[CH:5][CH:4]=[CH:3][C:20]2=5)[CH:7]=[CH:8][CH:9]=4)=[CH:12][CH:13]=[CH:14][C:15]3=[C:16]([CH:30]=[O:33])[CH:17]=1

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 947NitrogenHCID 9142PeryleneHCID 24287Tin tetrachlorideHCID 93323Bis(1,3-dichloroisopropyl ether)

生成物 1

HCID 36989163-Perylenecarboxaldehyde

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 72391,2-Dichlorobenzene溶媒

実験手順

A 3 L 3-neck flask fitted with overhead mechanical stirrer, thermometer, condenser, and N2 line was charged with perylene (Aldrich Chemical Co., Milwaukee, WI, 53201, 25 g, 99 mmol) and o-dichlorobenzene (500 mL). The liquid was warmed until all the large chunks of solid dissolved (80° ) and then cooled quickly to give finely divided crystals. After further cooling with a salt-ice bath to 5°, SnCl4 (Aldrich, 98%, 51.2 g, 0.897 mol, 23 mL), was added in one portion. No temperature change occurred. The pot temperature was kept below 5°, and 1,1-dichloromethylmethylether (Aldrich, 14.9 g, 0.13 mol, 11.7 mL) was added dropwise over 1 h. The resulting suspension was warmed slowly to 40° over 2 h and further stirred for 16 h. Considerable HCl gas evolution occurred during the warming and the early part of the reaction at 40°. The reaction mixture was then cooled to 10° and hydrolysed by careful addition of 1 L of cold H2O. After 4 h the layers were separated and the organic layer filtered, dried with anhydrous Na2SO4 (Mallinckrodt Co., 2nd and Mallinckrodt St., St. Louis, MO, 63147, 100 g) and filtered again. The clear yellow solution was passed through a 500 g plug of SiO2 using PhCH3 as the eluting solvent with 500 mL fractions. This chromatography separated unreacted perylene from the aldehyde and a more polar product. Fractions (5 L) containing the aldehyde were combined and the PhCH3 removed. The resulting oily solid was shaken with CH3OH (200 mL) and the orange-brown crystals which formed were collected by filtration to give after drying 23.2 g (83%) of 3-perylenecarbaldehyde mp 223°-233°, (C,H), (lit. mp 236°(darkens >230 °)), N. P. Buu-Hoi and C. T. Long, Recueil 75 1121 (1956).

後処理

  1. customA 3 L 3-neck flask fitted with overhead mechanical stirrer
  2. temperatureThe liquid was warmed until all the large chunks of solid
  3. dissolutiondissolved (80° )
  4. temperaturecooled quickly
  5. customto give finely divided crystals
  6. temperatureAfter further cooling with a salt-ice bath to 5°
  7. customwas kept below 5°
  8. temperatureThe resulting suspension was warmed slowly to 40° over 2 h
  9. customthe early part of the reaction at 40°
  10. customAfter 4 h the layers were separated
  11. filtrationthe organic layer filtered
  12. dry with materialdried with anhydrous Na2SO4 (Mallinckrodt Co., 2nd and Mallinckrodt St., St. Louis, MO, 63147, 100 g)
  13. filtrationfiltered again
  14. customThis chromatography separated unreacted perylene from the aldehyde
  15. additionFractions (5 L) containing the aldehyde
  16. customthe PhCH3 removed
  17. stirringThe resulting oily solid was shaken with CH3OH (200 mL)
  18. customthe orange-brown crystals which formed
  19. filtrationwere collected by filtration
  20. customto give
  21. dry with materialafter drying 23.2 g (83%) of 3-perylenecarbaldehyde mp 223°-233°, (C,H), (lit. mp 236°(darkens >230 °)), N

出典と根拠

ORDレコード
ord-eb83f3d6f7df4c058f46db88ebe9366b
出典データセット
uspto-grants-1985_07
特許番号
US04530800

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