ChemicalBook--->CAS DataBase List--->5469-33-0

5469-33-0

5469-33-0 Structure

5469-33-0 Structure
IdentificationBack Directory
[Name]

(IODOMETHYL)CYCLOHEXANE
[CAS]

5469-33-0
[Synonyms]

CYCLOHEXYLIODOMETHANE
(IODOMETHYL)CYCLOHEXANE
Cyclohexane, (iodoMethyl)-
Benzo[b]thiophene-2-carboxylicacid,5,8-dimethoxy-,methylester
[Molecular Formula]

C7H13I
[MDL Number]

MFCD06410739
[MOL File]

5469-33-0.mol
[Molecular Weight]

224.08
Chemical PropertiesBack Directory
[Melting point ]

175-178 °C
[Boiling point ]

86.5-87.5 °C(Press: 20-21 Torr)
[density ]

1.542 g/cm3(Temp: 14.2 °C)
[storage temp. ]

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

Colorless to light yellow Liquid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

(IODOMETHYL)CYCLOHEXANE(5469-33-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

Cyclohexanemethanol

100-49-2

(IODOMETHYL)CYCLOHEXANE

5469-33-0

Under nitrogen protection, cyclohexanemethanol (5.00 mL, 40.7 mmol) was dissolved in dichloromethane (101 mL) and cooled to 0 °C. Imidazole (3.6 g, 52.9 mmol), triphenylphosphine (13.9 g, 52.9 mmol) and iodine (13.4 g, 52.9 mmol) were added sequentially and the reaction mixture was stirred for 30 minutes. After completion of the reaction, dichloromethane was added to the reaction solution. The organic layer was washed sequentially with water and aqueous sodium thiosulfate, and the organic layer was dried with anhydrous sodium sulfate and subsequently concentrated. The concentrate was filtered through diatomaceous earth to further concentrate the filtrate. Finally, the crude product obtained was purified by silica gel column chromatography (80 g of silica gel, pentane as eluent) to give the colorless oily product (iodomethyl)cyclohexane (5.82 g, 64% yield).

[References]

[1] Patent: JP2017/119691, 2017, A. Location in patent: Paragraph 0179
[2] Chemische Berichte, 1907, vol. 40, p. 4865
[3] Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1906, vol. 142, p. 344
[4] Bulletin de la Societe Chimique de France, 1906, vol. <3> 35, p. 548
[5] Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1906, vol. 142, p. 344
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