Water → 3-Chloro-1-phenylpyrrolidin-2-one

HRID 855573ノート

反応式

HRID 855573 の反応式
[C:1]1([N:7]2[CH2:11][CH2:10][CH2:9][C:8]2=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Li+].C[Si]([N-][Si](C)(C)C)(C)C.S([Cl:33])(C1C=CC(C)=CC=1)(=O)=O.O>C1COCC1.CCOC(C)=O>[Cl:33][CH:9]1[CH2:10][CH2:11][N:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[C:8]1=[O:12]

参加物

7

反応物 4

HCID 962WaterHCID 73974-Toluenesulfonyl chlorideHCID 783751-Phenylpyrrolidin-2-oneHCID 2733832Lithium Hexamethyldisilazide

生成物 1

HCID 219355593-Chloro-1-phenylpyrrolidin-2-one

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒HCID 8857Ethyl Acetate溶媒

実験手順

1-Phenyl-2-pyrrolidinone (1 g, 6.2 mmol) in THF (60 mL, anhydrous) was cooled to −40° C. and LiHMDS (8 mL, 8 mmol, 1 M soln. in THF) was added. The resulting solution was stirred for 40 min. and tosyl chloride (1.78 g, 9.33 mmol) was then added. After warming the solution to RT over a 14 hour period, H2O added to quench reaction. The solution was then concentrated to provide an oil. Next, the oil was redissovled in EtOAc and washed with H2O and brine. The organic layer was dried over Na2SO4, filtered, and concentrated to an oil once again. Purified via flash column chromatography (4:1 hexane/EtOAc) provided 3-chloro-1-phenylpyrrolidin-2-one.

後処理

  1. additionadded
  2. customto quench
  3. customreaction
  4. concentrationThe solution was then concentrated
  5. customto provide an oil
  6. washwashed with H2O and brine
  7. dry with materialThe organic layer was dried over Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated to an oil once again
  10. customPurified via flash column chromatography (4:1 hexane/EtOAc)

出典と根拠

ORDレコード
ord-9b6bd28499c3486b8c1be729557a3056
出典データセット
uspto-grants-2007_08
特許番号
US07262198B2

反応ノート

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