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2-Amino-2-phenylpropanoic acid → 2-Amino-2-phenylpropan-1-ol

HRID 1911499
ノート
印刷プレビュー

反応式

HRID 1911499 の反応式
[NH2:1][C:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([CH3:6])[C:3](O)=[O:4].[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[NH2:1][C:2]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([CH3:6])[CH2:3][OH:4]
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 317222-Amino-2-phenylpropanoic acidHCID 21226445Aluminium lithium hydride

生成物 1

HCID 3497332-Amino-2-phenylpropan-1-ol収率 59.5%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred, cooled suspension of 2-amino-2-phenyl-propionic acid (488 mg) at r.t. in THF (10 ml) under an argon atmosphere was added portionwise LiAlH4 (244 mg). The ice bath was removed and stirring at r.t. was then continued for 20 h. The mixture was cooled in an ice bath, diluted with 5 ml THF and H2O (0.23 ml), 4 N NaOH (0.23 ml) and H2O (0.92 ml) were added successively and carefully. After 30 min stirring at r.t., the mixture was filtered and the cake was washed with THF. The filtrate was concentrated. The crude product was purified by column chromatography (silica gel; gradient: CH2Cl2->CH2Cl2/MeOH 9:1) to give 2-amino-2-phenyl-propan-1-ol (266 mg) as colorless viscous oil. MS (ISP): 152.3 ([M+H]+)

後処理

  1. temperatureTo a stirred, cooled
  2. customThe ice bath was removed
  3. temperatureThe mixture was cooled in an ice bath
  4. additiondiluted with 5 ml THF and H2O (0.23 ml), 4 N NaOH (0.23 ml) and H2O (0.92 ml)
  5. additionwere added successively
  6. stirringAfter 30 min stirring at r.t.
  7. filtrationthe mixture was filtered
  8. washthe cake was washed with THF
  9. concentrationThe filtrate was concentrated
  10. customThe crude product was purified by column chromatography (silica gel; gradient: CH2Cl2->CH2Cl2/MeOH 9:1)

出典と根拠

ORDレコード
ord-8017bd5b09104673b8972ec110dafeee
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08604061B2

反応ノート

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