Home Cart Sign in  
Chemical Structure| 10547-60-1 Chemical Structure| 10547-60-1

Structure of 10547-60-1

Chemical Structure| 10547-60-1

*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 [ 10547-60-1 ]

CAS No. :10547-60-1
Formula : C14H11ClO2
M.W : 246.69
SMILES Code : O=C(C1=CC=C(Cl)C=C1)C2=CC=C(OC)C=C2
MDL No. :MFCD01105071

Safety of [ 10547-60-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P270-P271-P280-P301+P312-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501

Application In Synthesis of [ 10547-60-1 ]

* 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 [ 10547-60-1 ]

[ 10547-60-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 42019-78-3 ]
  • CH3-halogen [ No CAS ]
  • [ 10547-60-1 ]
  • 2
  • [ 10547-60-1 ]
  • [ 42019-78-3 ]
YieldReaction ConditionsOperation in experiment
94% With hydrogen bromide; acetic acid; In water; at 125℃; 4-Chloro-4'-methoxybenzophenone of formula (IV) (0.1 mol, 24.7 g) was added to a 100 mL three-And add glacial acetic acid 30mL,Stirring plus 48percent of the mass fraction of HBr 10mL, heated to 125 ,Stirring reflux 4 ~ 5h.After concentration under reduced pressure to give a white solid,Add water to dissolve,Neutralized with aqueous NaOH to a pH of about 4,A white solid precipitated,Suction filtration,dry,Get its demethylation product,Ie, 21.90 g of 4-chloro-4'-hydroxybenzophenone of the formula (I)Product is a white solid,Yield 94percent.
90% With aluminum (III) chloride; In toluene; at 0 - 100℃; for 4h; General procedure: To a solution of 6a-c (1 eq.) in toluene was added aluminum chloride (1.2-2.0 eq.) at 0 °C. The resulting reaction mixture was refluxed for 4 h. The reaction mixture was allowed to cool to rt and then poured into 1 N HCl. The aqueous phase was extracted with EtOAc. The combined organic layer was washed with aq. NaHCO3 and brine, dried over Na2SO4 and filtered. The filtrate was concentrated under reduced pressure. This crude compound was crystallized from hexane.
85% With aluminum (III) chloride; In toluene; at 130℃; for 2h;Inert atmosphere; General procedure: AlCl3 (2.5 equiv.) was slowly added to a solution of 3b, 3d-l and 3n-p (1.0 equiv.) in toluene (0.15 M) under a N2 atmosphere. The mixture was refluxed at 130 °C for 2 h and by TLC (Pet. ether/EtOAc 4/1) full conversion was shown. The cooled mixture was poured into an 3 M HCl (aq.) solution, the organics were extracted with ethyl acetate (3 times), washed with brine, dried over MgSO4 and concentrated to give the desired 4-(benzoyl)phenols (4b, 4d-l and 4n-p) as solids.
74.21 g With copper(l) chloride; In hexane; at 60 - 85℃; for 3h;Reflux; Equipped with a stirrer, thermometer, reflux condenser, and dropping funnel, the reaction vessel with mass fraction of 85percent methylamine solution 500ml was added anisole 3.36 mol and cuprous chloride 0.37 mol. The stirring speed was controlled at 190 rpm. Control solution temperature 40°C. 0.35 mol of p-chlorobenzamide (3) was added dropwise. After the addition, the temperature of the solution was raised to 50°C. Maintain the stirring speed reaction 8h. The solution temperature was lowered to 35°C. The reaction solution was poured into the mass fraction of 35percent sodium bisulfite solution. The solution temperature was maintained at 5°C. The organic layer was separated. The aqueous layer was extracted 8 times with methylamine solution. After combining the organic layers, steaming methylamine, to give intermediate (4). Adding the mass fraction of 95percent hexane 300ml. Raising the temperature of the solution to 85°C. The solution temperature was reduced to 60°C. 0.6 mol of cuprous chloride was added. The reaction was refluxed for 3 h. The solution temperature was reduced to 9°C. Adding the mass fraction of 65percent potassium bicarbonate solution 200ml. The stirring speed was controlled at 260 rpm then fitered. Potassium sulfate solution. Solid sodium hydroxide dehydration, giving 4-chloro-4'-hydroxybenzophenone 74.21 g, yield 91percent.

 

Historical Records

Technical Information

Categories