ChemicalBook--->CAS DataBase List--->5632-15-5

5632-15-5

5632-15-5 Structure

5632-15-5 Structure
IdentificationMore
[Name]

2-Bromomethylquinoline
[CAS]

5632-15-5
[Synonyms]

2-(BROMOMETHYL)QUINOLINE,PURITY:95% MIN(HPLC)
2-(Bromomethyl)quinoline
2-Bromomethylquinoline
[Molecular Formula]

C10H8BrN
[MDL Number]

MFCD08062399
[Molecular Weight]

222.08
[MOL File]

5632-15-5.mol
Chemical PropertiesBack Directory
[Melting point ]

169 °C
[Boiling point ]

300.5±17.0 °C(Predicted)
[density ]

1.518±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

powder
[pka]

3.19±0.48(Predicted)
[Appearance]

Off-white to pink Solid
[BRN ]

115410
[InChI]

1S/C10H8BrN/c11-7-9-6-5-8-3-1-2-4-10(8)12-9/h1-6H,7H2
[InChIKey]

NNAYPIDFVQLEDK-UHFFFAOYSA-N
[SMILES]

BrCc1ccc2ccccc2n1
[CAS DataBase Reference]

5632-15-5(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H318
[Precautionary statements ]

P280-P301+P312+P330-P305+P351+P338+P310
[Hazard Codes ]

Xi
[Risk Statements ]

22-41-51/53
[Safety Statements ]

26-39-61
[RIDADR ]

3077
[WGK Germany ]

3
[HazardClass ]

9
[PackingGroup ]

Ⅲ
[HS Code ]

2933499090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Spectrum DetailBack Directory
[Spectrum Detail]

2-Bromomethylquinoline(5632-15-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

Quinaldine

91-63-4

2-Bromomethylquinoline

5632-15-5

GENERAL METHOD: 2-methylquinoline (0.5 mmol), cuprous halide (0.75 mmol), tert-butyl hydroperoxide (TBHP, 8.0 eq., 70% aqueous solution) and acetonitrile (CH3CN, 2 mL) were added to a reaction flask and the reaction was stirred for 8 hr at 70 °C. After completion of the reaction, the mixture was diluted with water and extracted with dichloromethane (CH2Cl2, 3 x 15 mL). The halogens (X2, X = I, Br, Cl) in the organic phase were quenched with sodium thiosulfate (Na2S2O3) solution. The organic layers were combined, washed with saturated aqueous ammonium chloride (NH4Cl) solution and dried over anhydrous sodium sulfate (Na2SO4). After filtration, the solvent was removed by concentration under reduced pressure. Finally, the target product 2-bromomethylquinoline was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, v/v = 10/1).

[References]

[1] Advanced Synthesis and Catalysis, 2018, vol. 360, # 21, p. 4197 - 4204
[2] Tetrahedron, 2018, vol. 74, # 15, p. 1908 - 1917
[3] Tetrahedron Letters, 2014, vol. 55, # 29, p. 3892 - 3895
[4] Chemical and Pharmaceutical Bulletin, 2000, vol. 48, # 4, p. 477 - 479
[5] Journal of Organometallic Chemistry, 2017, vol. 851, p. 194 - 209
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