Home Cart Sign in  
Chemical Structure| 150313-84-1 Chemical Structure| 150313-84-1

Structure of 150313-84-1

Chemical Structure| 150313-84-1

*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 [ 150313-84-1 ]

CAS No. :150313-84-1
Formula : C10H12BrNO3
M.W : 274.11
SMILES Code : OC1=C([N+]([O-])=O)C=C(Br)C=C1C(C)(C)C
MDL No. :MFCD27500713

Safety of [ 150313-84-1 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H315-H317-H318-H410
Precautionary Statements:P261-P264-P270-P272-P273-P280-P301+P312+P330-P302+P352-P305+P351+P338+P310-P333+P313-P391-P501
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 150313-84-1 ]

* 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 [ 150313-84-1 ]

[ 150313-84-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 10323-39-4 ]
  • [ 150313-84-1 ]
YieldReaction ConditionsOperation in experiment
52% With nitric acid; In hexane; at 20℃; for 4h; Step 2: 4-Bromo-2-(tert-butyl)-6-nitrophenol (9b) To a solution of compound 9a (10 g, 43.7 mmol) in hexane (62 mL) was slowly added HNO3 (2.3 mL) and then the solution was stirred at rt for 4 h. The resulting solution was taken up in Et2O, washed with water and sat. NaHCO3 solution, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by CC (elute: PE) to give compound 9b (6.2 g, 52%) as a yellow solid.
52% With nitric acid; In hexane; at 20℃; for 4h; Step 2: 4-Bromo-2-(tert-butyl)-6-nitrophenol (P9b)To a solution of compound P9a (10 g, 43.7 mmol) in hexane (62 mL) was slowly added HN03 (2.3 mL) and then the solution was stirred at rt for 4 h, diluted with Et20, washed with water and sat. NaHC03 solution, dried over Na2S04l filtered, concentrated and purified by CC (PE) to give compound P9b (6.2 g, 52%) as a yellow solid
With nitric acid; In hexane; at 0 - 20℃; for 2h; Concentrated nitric acid (112 ml) was gradually added dropwise to a solution of <strong>[10323-39-4]4-bromo-2-(tert-butyl)phenol</strong> (485 g) in hexane (3000 ml) while cooling on ice. After stirring for 2 hours at below 20C, ether (2000 ml) was added and the reaction mixture was washed with water. The organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. Hexane was added to the residue and the precipitated crystals were filtered to yield the title compound (418 g) as yellow crystals.1H-NMR(CDCl3)delta(ppm) 1.40(9H,s), 7.64(1H,d,J=2.4Hz), 8.14(1H,d,J=2.4Hz), 11.47(1H,s).
With sulfuric acid; sodium nitrite; In hexane; di-isopropyl ether; water; at 0 - 40℃; for 1h; step 2 Production of 4-bromo-2-tert-butyl-6-nitrophenol To a mixture of <strong>[10323-39-4]4-bromo-2-tert-butylphenol</strong> (41.6 g) and sodium nitrite (33.9 g) were added n-hexane (250 mL), diisopropyl ether (110 mL) and water (170 mL), and 4.5N sulfuric acid (350 mL) was added dropwise under ice-cooling. After stirring the mixture at room temperature for 1 hr, the reaction mixture was extracted with diisopropyl ether. The obtained diisopropyl ether layer was washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated, and the obtained residue was crystallized from n-hexane to give the title compound (23.0 g) as a yellow solid.

 

Historical Records