Identification | Back Directory | [Name]
2,4-DIMETHYLBENZYL BROMIDE | [CAS]
78831-87-5 | [Synonyms]
2,4-DIMETHYLBENZYL BROMIDE 2,4-Dimethylbenzyl bromide,98% 1-Bromomethyl-2,4-dimethylbenzene 2,4-DiMethylbenzyl broMide, 98% 1GR 1-(Bromomethyl)-2,4-dimethyl-benzene Benzene, 1-(bromomethyl)-2,4-dimethyl- Benzene, 1-(bromomethyl)-2,4-dimethyl- (7CI, 9CI) | [Molecular Formula]
C9H11Br | [MDL Number]
MFCD03844740 | [MOL File]
78831-87-5.mol | [Molecular Weight]
199.09 |
Chemical Properties | Back Directory | [Appearance]
clear colorless to light yellow liquid | [Melting point ]
15℃ | [Boiling point ]
235℃ | [density ]
1.314 | [refractive index ]
1.568-1.57
| [Fp ]
102℃ | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [form ]
Liquid | [color ]
Clear colorless to light yellow |
Hazard Information | Back Directory | [Chemical Properties]
clear colorless to light yellow liquid | [Synthesis]
General procedure for the synthesis of 2,4-dimethylbenzyl bromide from (2,4-dimethylphenyl)methanol:
1. to a solution of diisopropyl ether (100 mL) of (2,4-dimethylphenyl)methanol (10.77 g) was slowly added phosphorus tribromide (4.90 mL) at 0 °C.
2. The reaction mixture was stirred at room temperature for 1 hour.
3. Upon completion of the reaction, water was added to the mixture and extracted with ethyl acetate.
4. The organic phases were combined and washed twice with water, saturated aqueous sodium bicarbonate and saturated brine in that order.
5. The organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 2,4-dimethylbenzyl bromide as a colorless oil (15.5 g, quantitative yield).
6. The structure of the product was confirmed by 1H-NMR (CDCl3): δ 2.30 (3H, s), 2.37 (3H, s), 4.50 (2H, s), 6.96-6.99 (2H, m), 7.17-7.19 (1H, m). | [References]
[1] Patent: EP1787991, 2007, A1. Location in patent: Page/Page column 45 [2] Canadian Journal of Chemistry, 1986, vol. 64, p. 1060 - 1071 [3] Journal of Medicinal Chemistry, 1989, vol. 32, # 8, p. 1757 - 1763 [4] Polish Journal of Chemistry, 2007, vol. 81, # 5-6, p. 947 - 969 [5] Patent: US2007/129365, 2007, A1. Location in patent: Page/Page column 12 |
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