ChemicalBook--->CAS DataBase List--->873063-62-8

873063-62-8

873063-62-8 Structure

873063-62-8 Structure
IdentificationBack Directory
[Name]

Furan, tetrahydro-3-iodo-, (3R)-
[CAS]

873063-62-8
[Synonyms]

(3R)-3-Iodooxolane
Cholest-5-en-3-ol,(8α)-
(R)-3-Iodo-tetrahydrofuran
(3R)-3-Iodotetrahydrofuran
1-Butanesulfonicacid,8-hydroxy-
Furan, tetrahydro-3-iodo-, (3R)-
[Molecular Formula]

C4H7IO
[MDL Number]

MFCD17015957
[MOL File]

873063-62-8.mol
[Molecular Weight]

198
Chemical PropertiesBack Directory
[Boiling point ]

187.0±33.0 °C(Predicted)
[density ]

1.93±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C(protect from light)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[HS Code ]

2932190090
Spectrum DetailBack Directory
[Spectrum Detail]

Furan, tetrahydro-3-iodo-, (3R)-(873063-62-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

Furan, tetrahydro-3-iodo-, (3S)-

918439-76-6

Furan, tetrahydro-3-iodo-, (3R)-

873063-62-8

The general procedure for the synthesis of (R)-3-iodotetrahydrofuran from (S)-3-iodotetrahydrofuran was as follows: to a solution of (S)-tetrahydrofuran-3-ol (983 mg, 11.16 mmol) in dichloromethane (50 mL) was added triphenylphosphine (5.0 g, 21.20 mmol), glyoxal (1.4 g, 21.20 mmol) and iodine (5.0 g, 21.20 mmol). The reaction mixture was refluxed overnight, cooled and the reaction was quenched with saturated sodium thiosulfate solution. The organic layer was separated, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give a yellow solid. The solid was ground with hexane at room temperature for 2 h. The filtrate was concentrated after filtration. Finally, it was purified by silica gel column chromatography with ethyl acetate/hexane (0-5%) as eluent for 20 min to give (R)-3-iodotetrahydrofuran as a clear oil (1.0 g, 52% yield).

[References]

[1] Patent: WO2011/146287, 2011, A1. Location in patent: Page/Page column 120-121
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