Pyridine → HCID 14438699、化合物

HRID 1762781ノート

反応式

HRID 1762781 の反応式
[N:1]([CH2:8][CH2:9][OH:10])([CH2:5][CH2:6][OH:7])[CH2:2][CH2:3][OH:4].N1C=CC=CC=1.Cl[C:18]([C:20]1[C:32]2[C:31]3[C:26](=[CH:27][CH:28]=[CH:29][CH:30]=3)[C:25](=[C:33]([C:36]#[N:37])[C:34]#[N:35])[C:24]=2[CH:23]=[CH:22][CH:21]=1)=[O:19]>ClCCl>[C:36]([C:33]([C:34]#[N:35])=[C:25]1[C:24]2[CH:23]=[CH:22][CH:21]=[C:20]([C:18]([O:4][CH2:3][CH2:2][N:1]([CH2:8][CH2:9][OH:10])[CH2:5][CH2:6][OH:7])=[O:19])[C:32]=2[C:31]2[C:26]1=[CH:27][CH:28]=[CH:29][CH:30]=2)#[N:37]

参加物

5

反応物 3

HCID 1049PyridineHCID 7618TriethanolamineHCID 198332559-(Dicyanomethylidene)-9H-fluorene-4-carbonyl chloride

生成物 1

HCID 14438699HCID 14438699、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

A solution of 100.0 grams of triethanolamine and 58 milliliters of dry pyridine in 350 milliliters of dry dichloromethane was stirred at room temperature under a nitrogen atmosphere. A solution of 8.0 grams of (4-chloroformyl-9-fluorenylidene)malononitrile in 400 milliliters of dry dichloromethane was added over a period of 1 hour. After addition, the reaction mixture was further stirred for another hour. The reaction mixture was washed several times with water to remove the excess amines and the corresponding hydrochloride salts, dried with anhydrous magnesium sulfate and filtered. Evaporation of the filtrate gave 5 grams of crude product. Purification by recrystallization from isopropanol afforded 4.5 grams of pure (1c), mp., 155.5°-156.5° C.

後処理

  1. additionAfter addition
  2. washThe reaction mixture was washed several times with water
  3. customto remove the excess amines
  4. dry with materialthe corresponding hydrochloride salts, dried with anhydrous magnesium sulfate
  5. filtrationfiltered
  6. customEvaporation of the filtrate
  7. customgave 5 grams of crude product
  8. customPurification
  9. customby recrystallization from isopropanol

出典と根拠

ORDレコード
ord-9b8399d3cc134ac78069fbfb0fbd8d50
出典データセット
uspto-grants-1989_05
特許番号
US04835081

反応ノート

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