![](/StructureFile/ChemBookStructure8/GIF/CB1329078.gif)
1,3-DIBROMO-5-ISOPROPYLBENZENE synthesis
- Product Name:1,3-DIBROMO-5-ISOPROPYLBENZENE
- CAS Number:62655-20-3
- Molecular formula:C9H10Br2
- Molecular Weight:277.98
![2,6-DIBROMO-4-ISOPROPYLANILINE](/CAS/GIF/10546-65-3.gif)
10546-65-3
66 suppliers
$45.00/250mg
![1,3-DIBROMO-5-ISOPROPYLBENZENE](/StructureFile/ChemBookStructure8/GIF/CB1329078.gif)
62655-20-3
73 suppliers
$18.00/1g
Yield: 63%
Reaction Conditions:
Stage #1:2,6-dibromo-4-(1-methylethyl)benzenamine with sulfuric acid in ethanol at -5; for 0.25 h;
Stage #2: with sodium nitrite in ethanol at 80;
Steps:
1,3-Dibromo-5-isopropylbenzene (S13n)
To a mixtureof 500 mL of 96 % ethanol and 133 mL of 98 % H2SO4, 26.14g (89.2 mol) of 2,6-dibromo-4-isopropylaniline (S12n) was added withvigorous stirring at -5 °C over 15 min. Then, 16.864 g of NaNO2 wasadded at this temperature over 1 h, and the resulting mixture was stirred at 80°C overnight. Then, ice water was added to the reaction system and the organicproduct was extracted with 4 × 400 ml of dichloromethane. The combined extractwas dried over Na2SO4 and evaporated to get compound1,3-dibromo-5-isopropylbenzene (15.7 g, 63 %). 1H NMR (500 MHz, DMSO-d6) δ 7.59 (s, 1 H), 7.45 (d,2 H, J = 1.6 Hz), 2.92-2.85 (m, 1 H), 1.16 (d, 6 H, J = 6.8 Hz).
References:
Yu, Lei;Huang, Minhao;Xu, Tianfeng;Tong, Linjiang;Yan, Xiao-e;Zhang, Zhang;Xu, Yong;Yun, Caihong;Xie, Hua;Ding, Ke;Lu, Xiaoyun [European Journal of Medicinal Chemistry,2017,vol. 126,p. 1107 - 1117] Location in patent:supporting information
![4-Isopropylaniline](/CAS/GIF/99-88-7.gif)
99-88-7
206 suppliers
$8.00/5g
![1,3-DIBROMO-5-ISOPROPYLBENZENE](/StructureFile/ChemBookStructure8/GIF/CB1329078.gif)
62655-20-3
73 suppliers
$18.00/1g