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Hydrochloric Acid → 1-(4-Chlorophenyl)cyclobutanecarbaldehyde

HRID 1650931
ノート
印刷プレビュー

反応式

HRID 1650931 の反応式
[H-].C([Al+]CC(C)C)C(C)C.[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2([C:22]#N)[CH2:21][CH2:20][CH2:19]2)=[CH:14][CH:13]=1.Cl.CC[O:27]CC>CCCCCC>[Cl:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2([CH:22]=[O:27])[CH2:21][CH2:20][CH2:19]2)=[CH:14][CH:13]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 986211-(4-Chlorophenyl)cyclobutanecarbonitrileHCID 21225700Diisobutylaluminumhydride

生成物 1

HCID 99423881-(4-Chlorophenyl)cyclobutanecarbaldehyde

試薬・触媒・溶媒 1

HCID 8058Hexane溶媒

反応条件

温度
0 °C

実験手順

A 1M solution of diisobutylaluminium hydride in hexane (100 ml) was added dropwise to a stirred solution of 1-(4-chlorophenyl)cyclobutanecarbonitrile (19.1 g) in dry ether (50 ml) at -30° C. under nitrogen. The mixture was allowed to warm to 0° C. and was kept at that temperature for 30 minutes. The mixture was cooled to -30° C. and 5N hydrochloric acid (100 ml) was added dropwise with stirring. The mixture was filtered to separate a solid and the filtrate was extracted with ether. The solid was added to the ether extracts which were washed with water and dried. Removal of the solvent gave 1-(4-chlorophenyl)cyclobutanecarbaldehyde as a yellow oil.

後処理

  1. temperatureThe mixture was cooled to -30° C.
  2. filtrationThe mixture was filtered
  3. customto separate a solid
  4. extractionthe filtrate was extracted with ether
  5. additionThe solid was added to the ether extracts which
  6. washwere washed with water
  7. customdried
  8. customRemoval of the solvent

出典と根拠

ORDレコード
ord-2810d27f0e2549d3bfd218053aaef743
出典データセット
uspto-grants-1990_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04925879

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート