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ChemicalBook--->CAS DataBase List--->144870-96-2

144870-96-2

144870-96-2 Structure

144870-96-2 Structure
IdentificationBack Directory
[Name]

3-Furanol,4-aminotetrahydro-(9CI)
[CAS]

144870-96-2
[Synonyms]

4-aMinooxolan-3-ol
4-aminotetrahydro-3-Furanol
3-Furanol, 4-aMinotetrahydro-
3-Furanol,4-aminotetrahydro-(9CI)
[Molecular Formula]

C4H9NO2
[MDL Number]

MFCD11870199
[MOL File]

144870-96-2.mol
[Molecular Weight]

103.12
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

Light yellow to yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

3-Furanol,4-aminotetrahydro-(9CI)(144870-96-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

3,4-Epoxytetrahydrofuran

285-69-8

3-Furanol,4-aminotetrahydro-(9CI)

144870-96-2

The general procedure for the synthesis of 4-aminotetrahydrofuran-3-ol from 3,4-epoxytetrahydrofuran was as follows: 3,4-epoxytetrahydrofuran (0.3 g, 3.5 mmol) was dissolved in a mixture of isopropanol (5 mL) and ammonium hydroxide (10 mL), and the reaction was stirred for 15 hours at 80 °C. Upon completion of the reaction, the reaction mixture was quenched with water and subsequently extracted with ethyl acetate (EtOAc). The organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 4-aminotetrahydrofuran-3-ol (0.36 g, 100% yield). The product was analyzed by liquid chromatography-mass spectrometry (LC-MS) and showed m/z = 104.0 [M + H]+.

[References]

[1] Patent: WO2016/44770, 2016, A1. Location in patent: Page/Page column 726
[2] Patent: WO2008/33562, 2008, A2. Location in patent: Page/Page column 53
[3] Patent: US2009/76005, 2009, A1. Location in patent: Page/Page column 23
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