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Benzyl chloroformate → HCID 86623367、化合物

HRID 2089284
ノート
印刷プレビュー

反応式

HRID 2089284 の反応式
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:6][C@@H:7]([C:9]([OH:11])=O)[NH2:8].[H-].[H-].[H-].[H-].[Li+].[Al+3].[OH-].[Na+].Cl[C:21]([O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:22]>O1CCCC1.O>[OH:11][CH2:9][CH:7]([NH:8][C:21](=[O:22])[O:23][CH2:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)[CH2:6][C:2]1[S:1][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 10387Benzyl chloroformateHCID 14798Sodium Hydroxide2 回HCID 146719beta-2-Thienyl-L-alanineHCID 21226445Aluminium lithium hydride

生成物 1

HCID 86623367HCID 86623367、化合物収率 96.9%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

24.8 g of 3-(2-thienyl)alanine (144.8 mmol) were added in portions to 11.0 g of LiAlH4 in 550 ml of tetrahydrofuran, heated to reflux. The mixture was then heated under reflux for 8 hours and subsequently stirred at room temperature overnight. 17.6 ml of 10% NaOH solution were added and then 22 ml of H2O were slowly added dropwise, and the mixture was stirred for 5 minutes. Then, first 391 ml of 10% NaOH solution and subsequently, at −5° C., 22.2 g of benzyl chloroformate (130.32 mmol) were added, and the mixture was stirred at room temperature for 3 hours. For workup, the mixture was extracted with dichloromethane, the organic phase was dried, the solvent was evaporated and the remaining residue was filtered through silica gel (eluent: CH2Cl2/methanol 2.5%). 36.8 g of the title compound were obtained as a yellowish oil.

後処理

  1. temperatureheated to reflux
  2. temperatureThe mixture was then heated
  3. temperatureunder reflux for 8 hours
  4. stirringthe mixture was stirred for 5 minutes
  5. stirringthe mixture was stirred at room temperature for 3 hours
  6. extractionFor workup, the mixture was extracted with dichloromethane
  7. customthe organic phase was dried
  8. customthe solvent was evaporated
  9. filtrationthe remaining residue was filtered through silica gel (eluent: CH2Cl2/methanol 2.5%)

出典と根拠

ORDレコード
ord-130cf1e10eac4ea283d7601ca23015ae
出典データセット
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08436034B2

反応ノート

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