Home Cart Sign in  
Chemical Structure| 78782-27-1 Chemical Structure| 78782-27-1

Structure of 78782-27-1

Chemical Structure| 78782-27-1

*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 [ 78782-27-1 ]

CAS No. :78782-27-1
Formula : C14H19BO2
M.W : 230.11
SMILES Code : CC1(C)C(C)(C)OB(/C=C/C2=CC=CC=C2)O1
MDL No. :N/A

Safety of [ 78782-27-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 78782-27-1 ]

* 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 [ 78782-27-1 ]

[ 78782-27-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 618-89-3 ]
  • [ 78782-27-1 ]
  • [ 25692-41-5 ]
YieldReaction ConditionsOperation in experiment
82% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; 74A: 3-Styryl-benzoic acid methyl ester; Methyl 3-bromobenzoate (458 mg, 2 mmol), 1-styreneboronic acid pinacoyl ester (484 mg, 2.1 mmol), Na2CO3 (222 mg, 2.1 mmol), tetrakis(triphenylphosphino)palladium (116 mg, 0.1 mmol), water (4 mL) and 1,2-dimethoxyethane (6 mL) were stirred with reflux conditions for one hour, under nitrogen. The reaction mixture was diluted with water andwas extracted three times with EtOAc. The organic layers were combined, washed with water and then brine, dried over MgSO4 and concentrated. The product was purified by trituration with Et2O. White crystals were obtained (393 nig, 82 %). NMR 1U (ppm, CDC13): 8.19 (t, / = 1.6 Hz, 1H), 7.91 (dt, / = 7.7 Hz, / = 1.3 Hz, 1H), 7.67 (d, J3 = 7.8 Hz, 1H), 7.52 (d, J3 = 7.3 Hz, 2H), 7.42 (t, J3 = 7.9 Hz, 1H), 7.36 (t, J3 = 7.4 Hz, 2H), 7.30-7.26 (m, 1H), 7.19 (d, J3 = 16.3 Hz, 1H), 7.11 (d, / = 16.4 Hz, 1H), 3.06 (s, 3H).
82% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; for 1h;Heating / reflux; 74A: 3-Styryl-benzoic acid methyl ester; Methyl 3-bromobenzoate (458 mg, 2 mmol), 1-styreneboronic acid pinacoyl ester (484 mg, 2.1 mmol), Na2CO3 (222 mg, 2.1 mmol), tetrakis(triphenylphosphino)palladium (116 mg, 0.1 mmol), water (4 mL) and 1,2-dimethoxyethane (6 mL) were stirred with reflux conditions for one hour, under nitrogen. The reaction mixture was diluted with water and was extracted three times with EtOAc. The organic layers were combined, washed with water and then brine, dried over MgSO4 and concentrated. The product was purified by trituration with Et2O. White crystals were obtained (393 mg, 82%). NMR 1H (ppm, CDCl3): 8.19 (t, J4=1.6 Hz, 1H), 7.91 (dt, J3=7.7 Hz, J4=1.3 Hz, 1H), 7.67 (d, J3=7.8 Hz, 1H), 7.52 (d, J3=7.3 Hz, 2H), 7.42 (t, J3=7.9 Hz, 1H), 7.36 (t, J3=7.4 Hz, 2H), 7.30-7.26 (m, 1H), 7.19 (d, J3=16.3 Hz, 1H), 7.11 (d, J3=16.4 Hz, 1H), 3.06 (s, 3H).
 

Historical Records

Technical Information

Categories