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Sodium Iodide → 1-Bis(hydroxyethyl)amino-3-phenylthiopropane

HRID 344721
ノート
印刷プレビュー

反応式

HRID 344721 の反応式
Cl[CH2:2][CH2:3][CH2:4][S:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[NH:12]([CH2:16][CH2:17][OH:18])[CH2:13][CH2:14][OH:15].[I-].[Na+]>O1CCOCC1>[OH:15][CH2:14][CH2:13][N:12]([CH2:16][CH2:17][OH:18])[CH2:2][CH2:3][CH2:4][S:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=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 5238Sodium IodideHCID 8113DiethanolamineHCID 2696063-Chloropropyl phenyl sulfide

生成物 1

HCID 543093351-Bis(hydroxyethyl)amino-3-phenylthiopropane収率 57%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

A mixture of 8.30 g (44.5 mmols) of 1-chloro-3-phenylthiopropane, 100 ml of diethanolamine, 13.3 g (88.7 mmols) of sodium iodide and 250 ml of dioxan was heated under reflux for 15 hours. The mixture was concentrated under reduced pressure, and an aqueous saturated sodium bicarbonate solution was added to the mixture followed by extraction of the solution with chloroform 5 times. The chloroform layer was drided over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: chloroform/methanol =25/1) to afford 6.46 g (yield: 57%) of 1-bis(hydroxyethyl)amino-3-phenylthiopropane.

後処理

  1. temperaturewas heated
  2. temperatureunder reflux for 15 hours
  3. concentrationThe mixture was concentrated under reduced pressure
  4. additionan aqueous saturated sodium bicarbonate solution was added to the mixture
  5. extractionfollowed by extraction of the solution with chloroform 5 times
  6. customThe solvent was evaporated under reduced pressure
  7. customthe residue was purified by silica gel column chromatography (eluent: chloroform/methanol =25/1)

出典と根拠

ORDレコード
ord-a2e5d23f57bd405797d234b4f28b2055
出典データセット
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05053408

反応ノート

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