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Potassium Iodide → N-(2,6-dimethylphenyl)valine

HRID 648246
ノート
印刷プレビュー

反応式

HRID 648246 の反応式
Br[CH:2]([CH:20]([CH3:22])[CH3:21])[C:3]([O:5]CC1C=CC=C(OC2C=CC=CC=2)C=1)=[O:4].[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[C:25]=1[NH2:26].[I-].[K+]>S(=O)(=O)(O)O>[CH3:23][C:24]1[CH:30]=[CH:29][CH:28]=[C:27]([CH3:31])[C:25]=1[NH:26][C@H:2]([C:3]([OH:5])=[O:4])[CH:20]([CH3:22])[CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 4875Potassium IodideHCID 68962,6-DimethylanilineHCID 13229492m-Phenoxybenzyl alpha-bromoisovalerate

生成物 1

HCID 15383894N-(2,6-dimethylphenyl)valine

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

To m-phenoxybenzyl α-bromoisovalerate (2 g, 0.0055 mole), 24°, is added 2,6-dimethylaniline (3.33 g, 0.0275 mole) followed by a catalytic amount of potassium iodide (20 mg). The reaction mixture is heated at about 120° for 48 hours, and then poured into ice-water (20 ml) and 2 N sulfuric acid (10 ml) and extracted with ether (3×30 ml). The combined ether extracts are washed with water (2×20 ml) until neutral and with brine (10 ml) followed by drying over calcium sulfate. The reaction product is concentrated under vacuum and isolated by preparative TLC to give m-phenoxybenzyl ester of N-(2,6-dimethylphenyl)valine. MS m/e 403.2 (M+, 7.5).

後処理

  1. temperatureThe reaction mixture is heated at about 120° for 48 hours
  2. extractionextracted with ether (3×30 ml)
  3. washThe combined ether extracts are washed with water (2×20 ml) until neutral and with brine (10 ml)
  4. dry with materialby drying over calcium sulfate
  5. concentrationThe reaction product is concentrated under vacuum
  6. customisolated by preparative TLC

出典と根拠

ORDレコード
ord-c8307741d2bc43d89e84e8c13752c8d1
出典データセット
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04411912

反応ノート

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