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Dimethylamine → 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole

HRID 268524
ノート
印刷プレビュー

反応式

HRID 268524 の反応式
Cl[CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:8]=[CH:9][C:10]2[N:11]([CH2:26][CH3:27])[C:12]3[C:17]([C:18]=2[CH:19]=1)=[CH:16][C:15]([C:20](=[O:25])[CH2:21][CH2:22][CH2:23]Cl)=[CH:14][CH:13]=3)=[O:6].C([N:30]1[C:42]2C=CC=CC=2C2[C:31]1=CC=CC=2)C.ClCCCC(Cl)=O.[CH3:50][NH:51][CH3:52].[I-].[K+].[C:55]([OH:62])(=[O:61])/[CH:56]=[CH:57]/[C:58]([OH:60])=[O:59]>O1CCOCC1>[CH3:50][N:51]([CH3:52])[CH2:2][CH2:3][CH2:4][C:5]([C:7]1[CH:8]=[CH:9][C:10]2[N:11]([CH2:26][CH3:27])[C:12]3[C:17]([C:18]=2[CH:19]=1)=[CH:16][C:15]([C:20](=[O:25])[CH2:21][CH2:22][CH2:23][N:30]([CH3:42])[CH3:31])=[CH:14][CH:13]=3)=[O:6].[C:55]([O-:62])(=[O:61])/[CH:56]=[CH:57]/[C:58]([O-:60])=[O:59]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 6

HCID 674DimethylamineHCID 4875Potassium IodideHCID 6836N-ethyl carbazoleHCID 783704-Chlorobutyryl chlorideHCID 444972Fumaric AcidHCID 123317903,6-Bis(4-chlorobutyryl)-N-ethylcarbazole

生成物 2

HCID 461319
3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole
HCID 5460307Fumarate

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 15.8 g (0.039 mole) of 3,6-bis(4-chlorobutyryl)-N-ethylcarbazole, prepared from N-ethylcarbazole and 4-chlorobutyryl chloride, 75 ml of 40% aqueous dimethylamine and 2 g of potassium iodide in 175 ml of p-dioxane is heated in a reaction bomb with stirring for 44 hours. The reaction mixture is concentrated to one-half its original volume in vacuo and diluted with 500 ml of water. The semi-solid which separates is dissolved in ether and washed repeatedly with water and dried over magnesium sulfate to give the free base which is treated with fumaric acid and recrystallized from butanone to give 3,6-bis(4-dimethylaminobutyryl)-N-ethylcarbazole bis acid fumarate. M.P. 94°-98°C.

後処理

  1. temperatureis heated in a reaction bomb
  2. concentrationThe reaction mixture is concentrated to one-half its original volume in vacuo
  3. additiondiluted with 500 ml of water
  4. dissolutionThe semi-solid which separates is dissolved in ether
  5. washwashed repeatedly with water
  6. dry with materialdried over magnesium sulfate
  7. customto give the free base which
  8. customrecrystallized from butanone

出典と根拠

ORDレコード
ord-98dbf57019ff4ad687fba3e1257f67bf
出典データセット
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03947593

反応ノート

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