Cetylpyridinium Chloride → N-Hexadecylpyridinium 4-Cyanobenzenesulfinate

HRID 15614

反応式

HRID 15614 の反応式
[Cl-].[CH2:2]([N+:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17].[C:24]([C:26]1[CH:31]=[CH:30][C:29]([S:32]([O-:34])=[O:33])=[CH:28][CH:27]=1)#[N:25].[Na+]>C(O)C>[C:24]([C:26]1[CH:27]=[CH:28][C:29]([S:32]([O-:34])=[O:33])=[CH:30][CH:31]=1)#[N:25].[CH2:2]([N+:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH3:17]

参加物

4

反応物 2

HCID 31239Cetylpyridinium ChlorideHCID 23668300Sodium 4-cyanobenzenesulfinate

生成物 1

HCID 22055066N-Hexadecylpyridinium 4-Cyanobenzenesulfinate収率 108.3%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

A solution of N-hexadecylpyridinium chloride (1.6 g) in ethanol (20 mL) was added to an Erlenmeyer flask containing a magnetically stirred boiling solution of sodium 4-cyanobenzenesulfinate (1.0 g) in anhydrous ethanol (200 mL). The mixture was allowed to cool to room temperature and was then further cooled in an ice bath. The mixture was filtered and the filtrate was concentrated to dryness using a rotary evaporator. The residue was then dissolved in chloroform (100 mL), filtered, and concentrated to dryness using a rotary evaporator to afford 2.4 g of product.

後処理

  1. additioncontaining
  2. temperaturewas then further cooled in an ice bath
  3. filtrationThe mixture was filtered
  4. concentrationthe filtrate was concentrated to dryness
  5. customa rotary evaporator
  6. dissolutionThe residue was then dissolved in chloroform (100 mL)
  7. filtrationfiltered
  8. concentrationconcentrated to dryness
  9. customa rotary evaporator

出典と根拠

ORDレコード
ord-f0da4c5f987e4c8bbde8d540ddba5cfb
出典データセット
uspto-grants-2010_06
特許番号
US07732633B2

関連ノート

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