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Benzyl 3-phenylpropanoate → (S)-4-Isopropyl-2-phenethyl-4,5-dihydrooxazole

HRID 1365105
ノート
印刷プレビュー

反応式

HRID 1365105 の反応式
[C:1]1([CH2:7][CH2:8][C:9](OCC2C=CC=CC=2)=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[NH2:19][C@H:20]([CH2:24][OH:25])[CH:21]([CH3:23])[CH3:22]>ClC1C=CC=CC=1>[CH:21]([C@H:20]1[CH2:24][O:25][C:9]([CH2:8][CH2:7][C:1]2[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=2)=[N:19]1)([CH3:23])[CH3:22]
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 562789Benzyl 3-phenylpropanoateHCID 640993L-Valinol

生成物 1

HCID 13435839(S)-4-Isopropyl-2-phenethyl-4,5-dihydrooxazole収率 74%

試薬・触媒・溶媒 1

HCID 7964Chlorobenzene溶媒

実験手順

Under an argon atmosphere, a mixture of benzyl 3-phenylpropionate (1.5 mmol), (L)-valinol (1.8 mmol), Zn4(OCOCF3)6O (0.15 mmol) and chlorobenzene (2.5 mL) was heated under reflux for 18 hours. From the resulting solution, the solvent was removed using an evaporator, and the residues were purified by silica gel column chromatography to give (S)-4-isopropyl-2-(2-phenylethyl)-1,3-oxazoline in 74% yield. The compound was identified by comparison with physical property data of the known compound.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 18 hours
  3. customFrom the resulting solution, the solvent was removed
  4. customan evaporator
  5. customthe residues were purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-e60c0a1d60a14f5c8d97fe9ed1b937b8
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07888513B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート