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Hydrochloric Acid → (3S,5R)-5-Hydroxymethyl-1-(toluene-4-sulfonyl)-pyrrolidin-3-ol

HRID 906218
ノート
印刷プレビュー

反応式

HRID 906218 の反応式
C([O:3][C:4]([C@H:6]1[CH2:10][C@H:9]([O:11]C(=O)C)[CH2:8][N:7]1[S:15]([C:18]1[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=1)(=[O:17])=[O:16])=O)C.[H-].[H-].[H-].[H-].[Li+].[Al+3].Cl>C1COCC1>[OH:3][CH2:4][C@@H:6]1[N:7]([S:15]([C:18]2[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][CH:19]=2)(=[O:17])=[O:16])[CH2:8][C@@H:9]([OH:11])[CH2:10]1
参加物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 313Hydrochloric AcidHCID 15629284(2R,4S)-4-Acetoxy-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic Acid Ethyl EsterHCID 21226445Aluminium lithium hydride

生成物 1

HCID 15629267(3S,5R)-5-Hydroxymethyl-1-(toluene-4-sulfonyl)-pyrrolidin-3-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To an ice-cold solution of 4-acetoxy-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid ethyl ester (3) (0.65 g, 1.83 mmol) in THF (10 mL) is added LiAlH4 (0.135 g, 3.66 mmol) portion wise. Then the reaction mixture is stirred at room temperature for 1 h. After completion of the reaction, it is cooled to 0° C. and then pH of reaction mixture is adjusted to 3 by adding 6N HCl (0.65 mL). The mixture is concentrated, and the residue is triturated with water (8 mL), the solid precipitated out is filtered, washed with cold water (2×4 mL), and dried under reduced pressure to give compound (4) as white solid.

後処理

  1. customAfter completion of the reaction, it
  2. temperatureis cooled to 0° C.
  3. custompH of reaction mixture
  4. concentrationThe mixture is concentrated
  5. customthe residue is triturated with water (8 mL)
  6. customthe solid precipitated out
  7. filtrationis filtered
  8. washwashed with cold water (2×4 mL)
  9. customdried under reduced pressure

出典と根拠

ORDレコード
ord-5e8b703d5ad64ccea5cba31375c46931
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012983B2

反応ノート

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