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85531-02-8

85531-02-8 Structure

85531-02-8 Structure
IdentificationBack Directory
[Name]

5-(broMoMethyl)undecane
[CAS]

85531-02-8
[Synonyms]

C48Br
EA033
85531-02
5-(broMoMethyl)undecane
Undecane, 5-(bromomethyl)-
5-(broMoMethyl)undecane ISO 9001:2015 REACH
[Molecular Formula]

C12H25Br
[MDL Number]

MFCD23115881
[MOL File]

85531-02-8.mol
[Molecular Weight]

249.231
Chemical PropertiesBack Directory
[Boiling point ]

271.6±8.0 °C(Predicted)
[density ]

1.037±0.06 g/cm3(Predicted)
[refractive index ]

1.46
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

clear liquid to cloudy liquid
[color ]

Colorless to Light yellow
[InChI]

InChI=1S/C12H25Br/c1-3-5-7-8-10-12(11-13)9-6-4-2/h12H,3-11H2,1-2H3
[InChIKey]

PQAMWMMOUKNGEL-UHFFFAOYSA-N
[SMILES]

CCCCC(CBr)CCCCCC
[CAS DataBase Reference]

85531-02-8
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H227
[Precautionary statements ]

P501-P210-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313-P403+P235
[HS Code ]

2903.39.2050
Hazard InformationBack Directory
[Uses]

5-(Bromomethyl)-undecane is used as a reagent in the synthesis of alkyl triazole glycosides (ATGs) which is a new class of bio-related surfactants.
[Synthesis]

2-BUTYL-1-OCTANOL

3913-02-8

5-(broMoMethyl)undecane

85531-02-8

General procedure for the synthesis of 5-(bromomethyl)undecane from 2-butyl-octanol: Bromine (100 mmol, 5.11 mL) and triphenylphosphine (26.18 g, 100 mmol) were dissolved in 250 mL of dichloromethane (DCM) and bubbled with argon (Ar) for 10 min. The reaction system was cooled to 0 °C, followed by the addition of 2-butyl-1-octanol (18.635 g, 100 mmol) and stirred at this temperature for 30 min, then at room temperature overnight. After completion of the reaction, a small amount of sodium carbonate (Na2CO3) was added to the reaction mixture. The solvent was removed by distillation under reduced pressure and the residue was filtered and washed with hexane. The crude product was purified by silica gel column chromatography using petroleum ether (PE) as eluent to give a colorless oily product (22.0 g, 88.1% yield). The structure of the product was confirmed by nuclear magnetic resonance hydrogen (1H NMR, 400 MHz, CDCl3) and carbon (13C NMR, 125 MHz, CDCl3) spectra: 1H NMR (400 MHz, CDCl3) δ 3.45 (d, J = 4.8 Hz, 2H), 1.59 (dd, J = 11.1, 5.3 Hz, 1H), 1.40- 1.21 (m, 16H), 0.90 (q, J = 6.9 Hz, 6H); 13C NMR (125 MHz, CDCl3) δ 39.88, 39.62, 32.71, 32.40, 31.95, 29.61, 28.92, 26.68, 22.99, 22.80, 14.25, 14.21.

[References]

[1] New Journal of Chemistry, 2017, vol. 41, # 8, p. 2899 - 2909
[2] Patent: WO2017/152354, 2017, A1. Location in patent: Page/Page column 44; 45
[3] Journal of the American Chemical Society, 2011, vol. 133, # 10, p. 3284 - 3287
[4] Chemische Berichte, 1929, vol. 62, p. 2883
[5] Journal of Organic Chemistry, 1960, vol. 25, p. 665 - 666
Spectrum DetailBack Directory
[Spectrum Detail]

5-(broMoMethyl)undecane(85531-02-8)1HNMR
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