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Benzhydrylamine → Ethyl (2S,3S)-3-diphenylmethylcarbamoyloxirane-2-carboxylate

HRID 1456610
ノート
印刷プレビュー

反応式

HRID 1456610 の反応式
[CH2:1]([O:3][C:4]([C@H:6]1[O:8][C@@H:7]1[C:9]([OH:11])=O)=[O:5])[CH3:2].ON1C(=O)CCC1=O.C1(N=C=NC2CCCCC2)CCCCC1.[NH2:35][CH:36]([C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1>C(OCC)(=O)C.CCCCCC>[C:37]1([CH:36]([NH:35][C:9]([C@H:7]2[O:8][C@@H:6]2[C:4]([O:3][CH2:1][CH3:2])=[O:5])=[O:11])[C:43]2[CH:44]=[CH:45][CH:46]=[CH:47][CH:48]=2)[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1
参加物反応条件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 7036BenzhydrylamineHCID 10868DicyclohexylcarbodiimideHCID 80170N-HydroxysuccinimideHCID 11030109(2S,3S)-3-(ethoxycarbonyl)oxirane-2-carboxylic acid

生成物 1

HCID 57291692Ethyl (2S,3S)-3-diphenylmethylcarbamoyloxirane-2-carboxylate

試薬・触媒・溶媒 2

HCID 8058
Hexane
溶媒
HCID 8857Ethyl Acetate溶媒2 回

反応条件

温度
5 °C

実験手順

To a solution of (2S,3S)-3-ethoxycarbonyloxirane-2-carboxylic acid (8.01 g, 50.0 mmol.) in ethyl acetate (120 mL) was added N-hydroxysuccinimide (5.76 g, 50.0 mmol.) and then added N,N'-dicyclohexylcarbodiimide (5.75 g, 50.0 mmol) under chilling with ice. The resulting mixture was stirred at 5° C. for one hour, and to the mixture was a solution of aminodiphenylmethane (9.17 g, 50.0 mmol.) in ethyl acetate (30 mL). The mixture was stirred at 5° C. for one hour and then at room temperature for one hour. The resulting N,N'-dicyclohexylurea (DC-Urea) was removed by filtration, and the filtrate was washed successively with 1N hydrochloric acid, an aqueous sodium hydrogen carbonate saturated solution, and an aqueous sodium chloride saturated solution, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was recrystalized from ethyl acetate--n-hexane, to give the desired compound as a white crystalline product (1.25 g, yield: 77%).

後処理

  1. stirringThe mixture was stirred at 5° C. for one hour
  2. waitat room temperature for one hour
  3. customThe resulting N,N'-dicyclohexylurea (DC-Urea) was removed by filtration
  4. washthe filtrate was washed successively with 1N hydrochloric acid
  5. dry with materialan aqueous sodium hydrogen carbonate saturated solution, and an aqueous sodium chloride saturated solution, and then dried over anhydrous sodium sulfate
  6. distillationThe solvent was distilled off under reduced pressure
  7. customthe residue was recrystalized from ethyl acetate

出典と根拠

ORDレコード
ord-320293505c3847a19e7a6b4387c7b2cf
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05843992

反応ノート

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