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Triphenylphosphine → HCID 69006959、化合物

HRID 1432047
ノート
印刷プレビュー

反応式

HRID 1432047 の反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([I:9])=[C:6]([OH:8])[CH:7]=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C.[C:43]([O:47][C:48]([C@@H:50]1[CH2:54][CH2:53][CH2:52][N:51]1[CH2:55][CH2:56]O)=[O:49])([CH3:46])([CH3:45])[CH3:44]>C1COCC1>[C:43]([O:47][C:48]([C@@H:50]1[CH2:54][CH2:53][CH2:52][N:51]1[CH2:55][CH2:56][O:8][C:6]1[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=1[I:9])=[O:49])([CH3:46])([CH3:45])[CH3:44]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11776TriphenylphosphineHCID 5363146Diisopropyl azodicarboxylateHCID 66133335-Chloro-2-iodophenolHCID 690063851-(2-hydroxy-ethyl)-pyrrolidine-2-(S)-carboxylic acid tertbutyl ester

生成物 1

HCID 69006959HCID 69006959、化合物

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒
2 回

実験手順

5-Chloro-2-iodophenol (801 mg, 3.15 mmol) and PPh3 (1.15 g, 4.41 mmol) were dissolved in THF (25 mL). DIAD (0.91 mL, 4.62 mmol). was added dropwise and the solution was stirred for 20 min. A solution of 1-(2-hydroxy-ethyl)-pyrrolidine-2-(S)-carboxylic acid tert butyl ester (816 mg, 3.79 mmol) in THF (4 mL) was added via canulation. The mixture was stirred for 40 min at 0° C. then for 1.5 h at room temperature and finally for 3 h at 50° C. The mixture was diluted with heptanes (100 mL), washed with water (4×25 mL), dried over Na2SO4 and evaporated onto silica gel. After flash chromatography using silica gel, eluting with heptanes/EtOAc, 9:1, the title compound was obtained as a colorless oil (1.023 g, 72%).

後処理

  1. additionwas added dropwise
  2. stirringThe mixture was stirred for 40 min at 0° C.
  3. waitfor 1.5 h at room temperature
  4. waitfinally for 3 h at 50° C
  5. washwashed with water (4×25 mL)
  6. dry with materialdried over Na2SO4
  7. customevaporated onto silica gel
  8. washeluting with heptanes/EtOAc, 9:1

出典と根拠

ORDレコード
ord-1e77f6fb2dd3418984eac637e48d6d6f
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07612068B2

反応ノート

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