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Cyclohexylamine → HCID 10469811、化合物

HRID 1756019
ノート
印刷プレビュー

反応式

HRID 1756019 の反応式
[CH:1]1([NH2:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Br:8][CH:9]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:10](Cl)=[O:11]>C(Cl)(Cl)Cl>[CH:1]1([NH:7][C:10](=[O:11])[CH:9]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[Br:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 7965CyclohexylamineHCID 598182Bromophenylacetyl chloride

生成物 1

HCID 10469811HCID 10469811、化合物収率 41.3%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To a mixture of cyclohexylamine (10.9 g), triethylemine (11.1 g) and chloroform (200 ml), α-bromophenylacetyl chloride (23.3 g) was added dropwise over 10 minutes under cooling with ice and stirring, and the mixture was refluxed for 10 hours. After cooling by allowing to stand, the reaction mixture was washed with 0.5N hydrochloric acid (100 ml), with 0.5N aqueous solution of sodium hydroxide (100 ml) and with saturated saline solution (100 ml), and then concentrated. The residue was recrystallized from ethyl acetate-ethanol to obtain 12.2 g of title compound as colorless crystals. The mother liquor from recrystallization was concentrated and the residue was purified by means of column chromatography (developing solvent, chloroform:ethanol=20 : 1) to obtain 13.0 g of additional. title compound as colorless crystals (overall yield 85.4%).

後処理

  1. additionwas added dropwise over 10 minutes
  2. temperatureunder cooling with ice
  3. temperaturethe mixture was refluxed for 10 hours
  4. temperatureAfter cooling
  5. washthe reaction mixture was washed with 0.5N hydrochloric acid (100 ml), with 0.5N aqueous solution of sodium hydroxide (100 ml) and with saturated saline solution (100 ml)
  6. concentrationconcentrated
  7. customThe residue was recrystallized from ethyl acetate-ethanol

出典と根拠

ORDレコード
ord-58c0bfa26a1e40f5a26d450545ae3635
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05439919

反応ノート

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