Home Cart Sign in  
Chemical Structure| 1381846-22-5 Chemical Structure| 1381846-22-5

Structure of 1381846-22-5

Chemical Structure| 1381846-22-5

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1381846-22-5 ]

CAS No. :1381846-22-5
Formula : C8H4Br3N
M.W : 353.84
SMILES Code : N#CC1=CC=C(C(Br)Br)C(Br)=C1

Safety of [ 1381846-22-5 ]

Application In Synthesis of [ 1381846-22-5 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1381846-22-5 ]

[ 1381846-22-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 42872-74-2 ]
  • [ 1381846-22-5 ]
YieldReaction ConditionsOperation in experiment
97.5% With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 48h;Reflux; A solution of <strong>[42872-74-2]3-bromo-4-methyl-benzonitrile</strong> (5.00 g, 25.5 mmol) was dissolved in CCl4 (170 mL) and successively treated with NBS (18.2 g, 102 mmol) and benzoyl peroxide (0618 g, 2.55 mmol) at ambient temperature. The resulting solution was warmed to reflux, maintained 48 h then cooled to ambient temperature and filtered through a scintered glass funnel of medium porosity. The filtrate was concentrated, and the crude orange solid thus obtained purified by chromatography on silica using 49:1 hexanes/EtOAc to afford the title compound as a white solid (8.80 g, 24.9 mmol; 97.5%).
89.6% With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 14h;Reflux; Dissolve <strong>[42872-74-2]3-bromo-4-methylbenzonitrile</strong> (10g, 51mmol) in carbon tetrachloride (100mL), add NBS (22.6g, 127.5mmol) and benzoyl peroxide (272mg, 2.5mmol), and reflux 14h, the raw materials disappeared. Cool to room temperature, add water (400 mL), extract with DCM (200 mL × 2), and obtain column chromatography (P / E = 20: 1) to obtain 16.17 g of white solid with a yield of 89.6% and melting point: 48-49 C.
82% With N-Bromosuccinimide; In tetrachloromethane; at 95℃; for 48h; Preparation 13-Bromo-4-(dibromomethyl)benzonitrileHeat a mixture of <strong>[42872-74-2]3-bromo-4-methylbenzonitrile</strong> (25.0 g, 127.5 mmol, 1.0 equiv) and NBS (5.53 g, 306.1 mmol, 2.4 equiv) in carbon tetrachloride (200 mL) to 95 C. for two days. Cool the resulting suspension and remove the solids by filtration. Concentrate the filtrate under reduced pressure, and subject the resulting crude material to chromatography on silica gel eluting with a 2-5% THF/hexanes gradient to give the title compound (37.09 g, 82%). 1H NMR (CDCl3, 400 MHz): delta 8.10 (d, 1H, J=8.2 Hz), 7.79 (d, 1H, J=1.3 Hz), 7.67 (dd, 1H, J=8.2, 1.3 Hz), 6.99 (s, 1H).
82% With N-Bromosuccinimide; In tetrachloromethane; at 95℃; for 48h; Heat a mixture of <strong>[42872-74-2]3-bromo-4-methylbenzonitrile</strong> (25.0 g, 127.5 mmol, 1.0 equiv) and n-bromosuccinimide (NBS) (5.53 g, 306.1 mmol, 2.4 equiv) in carbon tetrachloride (200 mL) to 95 C. for two days. Cool the resulting suspension, and remove the solids by filtration. Concentrate the filtrate under reduced pressure, and purify the resulting crude material by chromatography on silica gel eluting with a gradient of 2-5% THF/hexanes to furnish the title compound (37.09 g, 82% yield). 1H NMR (400 MHz, CDCl3) delta 8.10 (d, 1H, J=8.2 Hz), 7.79 (d, 1H, J=1.3 Hz), 7.67 (dd, 1H, J=8.2, 1.3 Hz), 6.99 (s, 1H).

  • 2
  • [ 1381846-22-5 ]
  • [ 89891-69-0 ]
YieldReaction ConditionsOperation in experiment
59.3% With dimethyl sulfoxide; In water; at 120℃; for 6.0h; A solution of the product of Part 3A (8.80 g, 24.9 mmol) was dissolved in wet DMSO (83 mL) at ambient temperature then warmed to 120 °C and maintained 6 h. After cooling to ambient temperature, the resulting solution was diluted with H2O with transfer to a separatory funnel then washed EtOAc. The EtOAc solution was separated, washed with H2O and saturated aqueous NaCl then dried over Na2SO4, filtered and concentrated in vacuo to a yellow solid. Subsequent purification by chromatography on silica using 20: 1 hexanes/EtOAc afforded the title compound as a white solid (3.10 g, 14.8 mmol; 59.3percent).
 

Historical Records