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

HRID 344721
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HRID 344721 반응식
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
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참가 물질

5

반응물 3

HCID 5238Sodium IodideHCID 8113DiethanolamineHCID 2696063-Chloropropyl phenyl sulfide

생성물 1

HCID 543093351-Bis(hydroxyethyl)amino-3-phenylthiopropane수율 57%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-a2e5d23f57bd405797d234b4f28b2055
출처 데이터셋
uspto-grants-1991_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05053408

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