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Ammonium formate → (S)-N-[2-(2,3-dihydrobenzofuran-5-yl)-1-methylethyl]ethylamine

HRID 429815
ノート
印刷プレビュー

反応式

HRID 429815 の反応式
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C@@H:11]([N:13]([C@H](C3C=CC=CC=3)C)[CH2:14][CH3:15])[CH3:12])=[CH:9][C:4]=2[CH2:3][CH2:2]1.C([O-])=O.[NH4+]>[Pd].C(O)C>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C@@H:11]([NH:13][CH2:14][CH3:15])[CH3:12])=[CH:9][C:4]=2[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

5

反応物 2

HCID 2723923Ammonium formateHCID 57246230(S,S)-N-[2-(2,3-dihydrobenzofuran-5-yl)-1-methylethyl]-N-ethyl-(1-phenylethyl)amine

生成物 1

HCID 11106515(S)-N-[2-(2,3-dihydrobenzofuran-5-yl)-1-methylethyl]ethylamine収率 92.2%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

A mixture of (S,S)-N-[2-(2,3-dihydrobenzofuran-5-yl)-1-methylethyl]-N-ethyl-(1-phenylethyl)amine (23 grams, 0.074 mole) and ammonium formate (30 grams, 0.48 mole) and 10% palladium on carbon (3.7 grams) in ethanol (300 ml) was heated under reflux for 2 hours. The mixture was filtered and the solvent was evaporated to give a residue which was partitioned between 5% sodium hydroxide and ether. Evaporation of the organic phase gave (S)-N-[2-(2,3-dihydrobenzofuran-5-yl)-1-methylethyl]ethylamine as an oil (14 grams, 92%), M+ 205.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hours
  3. filtrationThe mixture was filtered
  4. customthe solvent was evaporated
  5. customto give a residue which
  6. customwas partitioned between 5% sodium hydroxide and ether
  7. customEvaporation of the organic phase

出典と根拠

ORDレコード
ord-ea39330baf954d839574e6dd8c88c934
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06319920B1

反応ノート

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