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Ethylene Oxide → N-[2-(1,1-Dimethylethoxy)-2-oxoethyl]-N-(2-hydroxyethyl)-L-tryptophan 1,1-dimethylethyl ester

HRID 2185590
ノート
印刷プレビュー

反応式

HRID 2185590 の反応式
[CH3:1][C:2]([O:5][C:6](=[O:27])[C@H:7]([CH2:17][C:18]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[NH:20][CH:19]=1)[NH:8][CH2:9][C:10]([O:12][C:13]([CH3:16])([CH3:15])[CH3:14])=[O:11])([CH3:4])[CH3:3].[CH2:28]1[O:30][CH2:29]1.[O-]S(C(F)(F)F)(=O)=O.[Yb+3].[O-]S(C(F)(F)F)(=O)=O.[O-]S(C(F)(F)F)(=O)=O>CC#N>[CH3:4][C:2]([O:5][C:6](=[O:27])[C@H:7]([CH2:17][C:18]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[NH:20][CH:19]=1)[N:8]([CH2:9][C:10]([O:12][C:13]([CH3:14])([CH3:15])[CH3:16])=[O:11])[CH2:28][CH2:29][OH:30])([CH3:1])[CH3:3]
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

5

反応物 3

HCID 6354Ethylene OxideHCID 2733225Ytterbium triflateHCID 53674071N-[2-(1,1-Dimethylethoxy)-2-oxoethyl]-L-tryptophan 1,1-dimethylethyl ester

生成物 1

HCID 69778108N-[2-(1,1-Dimethylethoxy)-2-oxoethyl]-N-(2-hydroxyethyl)-L-tryptophan 1,1-dimethylethyl ester収率 77.3%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile
溶媒

反応条件

温度
-80 °C

実験手順

In a four-necked flask cooled to −80° C. equipped with a mechanical stirrer, a thermometer, and a jacketed dropping funnel N-[2-(1,1-dimethylethoxy)-2-oxoethyl]-L-tryptophan 1,1-dimethylethyl ester (5 g; 13.35 mmol) was dissolved in CH3CN (25 mL). In the dropping funnel, cooled at −80° C., ethylene oxide (13 mL; 0.26 mol) was collected from the cylinder and then quickly dropped into the solution. Solid ytterbium triflate (0.83 g; 1.34 mmol) was added and after removal of the cooling bath the temperature was allowed to rise to r.t. The reaction was monitored by HPLC (Chromatographic method of Example 3, A)). After 15 h the solution was diluted with H2O (50 mL) and extracted with Et2O (150 mL). After evaporation of the solvent the crude was purified by flash chromatography (silica gel; n-hexane/ethyl acetate, 7:3 v/v) giving the desired product (4.32 g; 10.32 mmol).

後処理

  1. customequipped with a mechanical stirrer
  2. temperatureIn the dropping funnel, cooled at −80° C.
  3. additionquickly dropped into the solution
  4. customafter removal of the cooling bath the temperature
  5. customto rise to r.t
  6. additionAfter 15 h the solution was diluted with H2O (50 mL)
  7. extractionextracted with Et2O (150 mL)
  8. customAfter evaporation of the solvent the crude
  9. customwas purified by flash chromatography (silica gel; n-hexane/ethyl acetate, 7:3 v/v)

出典と根拠

ORDレコード
ord-f7a36c515134449da8f567efa37d3746
出典データセット
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06403055B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート