ChemicalBook--->CAS DataBase List--->39959-51-8

39959-51-8

39959-51-8 Structure

39959-51-8 Structure
IdentificationBack Directory
[Name]

2-IODOBENZYLAMINE
[CAS]

39959-51-8
[Synonyms]

2-IODOBENZYLAMINE
RARECHEM AL BW 0704
2-Iodobenzenemethanamine
(2-Iodophenyl)MethanaMine
BenzeneMethanaMine, 2-iodo-
1-(2-iodophenyl)methanamine
[Molecular Formula]

C7H8IN
[MDL Number]

MFCD00047929
[MOL File]

39959-51-8.mol
[Molecular Weight]

233.05
Chemical PropertiesBack Directory
[Melting point ]

63-65 °C
[Boiling point ]

270.0±15.0 °C(Predicted)
[density ]

1.772±0.06 g/cm3(Predicted)
[storage temp. ]

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

8.54±0.10(Predicted)
[Appearance]

Light yellow to brown Liquid
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P501-P260-P264-P280-P303+P361+P353-P301+P330+P331-P363-P304+P340+P310-P305+P351+P338+P310-P405
Spectrum DetailBack Directory
[Spectrum Detail]

2-IODOBENZYLAMINE(39959-51-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-(Azidomethyl)-2-iodobenzene

405198-82-5

2-IODOBENZYLAMINE

39959-51-8

Triphenylphosphine (6.8 g, 25.7 mmol) was added to an anhydrous tetrahydrofuran (THF, 100 mL) solution of 1-azidomethyl-2-iodobenzene (6.1 g, 23.4 mmol) at 0 °C. The reaction mixture was slowly warmed to room temperature and stirred for 16 hours. After the reaction was completed, the reaction mixture was diluted with ammonium hydroxide (20 mL) and stirring was continued for 3 hours. Subsequently, the reaction mixture was treated with 2M sodium hydroxide solution (30 mL) and stirred for another 1 hour. The reaction mixture was acidified to pH 2 with 3M hydrochloric acid, then diluted with ether and the layers were separated. The aqueous layer was alkalized to pH 9 with 2M sodium hydroxide solution and subsequently extracted with dichloromethane (3 times). The organic phases were combined, dried with anhydrous sodium sulfate and concentrated under vacuum to give an oily residue. The residue was treated with ether and filtered. The filtrate was purified by silica gel column chromatography using 95:5 dichloromethane:methanol as eluent to give 5.4 g (80% yield) of 2-iodobenzylamine.

[References]

[1] Patent: US2006/25433, 2006, A1. Location in patent: Page/Page column 107
[2] Tetrahedron, 2001, vol. 57, # 48, p. 9697 - 9710
[3] Angewandte Chemie - International Edition, 2005, vol. 44, # 35, p. 5679 - 5682
[4] Patent: US2006/24834, 2006, A1. Location in patent: Page/Page column 5-6; Sheet 7
[5] Journal of Organic Chemistry, 2010, vol. 75, # 24, p. 8410 - 8415
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