Home Cart Sign in  
Chemical Structure| 84542-11-0 Chemical Structure| 84542-11-0

Structure of 84542-11-0

Chemical Structure| 84542-11-0

*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 [ 84542-11-0 ]

CAS No. :84542-11-0
Formula : C12H14O3
M.W : 206.24
SMILES Code : CC(C)(C1=CC=C(C=O)C=C1)C(OC)=O
MDL No. :MFCD26383800

Safety of [ 84542-11-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 84542-11-0 ]

* 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 [ 84542-11-0 ]

[ 84542-11-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 557-21-1 ]
  • [ 57625-74-8 ]
  • [ 84542-11-0 ]
YieldReaction ConditionsOperation in experiment
Into a 250-ML THREE-NECKED FLASK there were placed 2.5 g of 2-PHENYL-2-METHYL propionic acid methyl ester and 2.4 g of zinc cyanide and 100 ml of tetrachloroethane. A strong flow of hydrogen chloride was introduced into the flask with intense stirring during 4 hours. The flask was cooled down with an ice bath and 4.8 g of finely divided aluminium chloride were added in one dose with continued intense stirring. The stirring continued for another thirty minutes and the flask was placed onto an oil bath where it was gradually heated up to the temperature of 70 C. Further on, the mixture was kept at the given temperature for three hours. After cooling with running water, the contents of the flask were poured onto crushed ICE/15M1 conc. HCI. The reaction mixture was left to stand overnight. Then it was transferred to the flask where it was REFLUXED for three hours and after cooling, it was divided in a separatory funnel. The organic layer was separated; the aqueous layer was extracted with 15 mi of TETRACHLOROETHANE. The combined organic extracts were washed with water, with 10% sodium carbonate and dried over sodium sulphate. The solvent was distilled off until 1/3 of the volume and the product was filtered through a short column of silica gel. 2. 1 G of the product were obtained having 92.6% GC purity.
  • 2
  • [ 4885-02-3 ]
  • [ 57625-74-8 ]
  • [ 84542-11-0 ]
YieldReaction ConditionsOperation in experiment
titanium tetrachloride; In dichloromethane; at 0 - 20℃; for 16.25h; 2-(4-Formyl-phenyl)-2-methyl-propionic acid methyl ester 6.80 g (38 mmol) of 2-methyl-2-phenyl-propionic acid methyl ester was dissolved at rt in 200 mL MeCl2 and 7.01 ml (90.4 g=76 mmol) of dichloromethylmethylether was added and the mixture cooled down to 0 C.; 21.47 mL (36.93 g=191 mmol) TiCl4 was added over 15 min and the reaction warmed up to ambient temperature; stirring was continued for 16 hours. The reaction mixture was then treated at 0 C. with 20 ml of HCl (37% in water) and extracted twice with MeCl2; the organic phases were washed with water, dried over MgSO4, filtered and evaporated. The crude product was purified by chromatography (silicagel, eluent:gradient of n-heptane/EtOAc) to yield 5.00 g of the title compound as yellow oil. MS: 206.1 (M+).
0.1 g To a solution of intermediate 39c (1 .0 g, 1 .0 eq) in DCM (30 mL) at 0 00 TiCI4 (5.3 g,5.0 eq) was added and stirred a room temperature for 30 mm. Then,dichloromethylmethyl ether (3.22 g, 5.0 eq) was added under cooling and stirred at room temperature over night. The reaction mixture was quenched with 1 N HCI (PH=3) and extracted with ethyl acetate, washed with water and dried. The product was obtained by concentrating under vacuo. The product was purified by combif lashto yield the title compound (0.1 g) as a colourless liquid. 1H NMR: (ODd3, 300MHz) 69.93 (d, 4H) 7.77-7.80 (d, 2H), 7.42-7.45 (d, 1 H), 3.60 (5, 3H), 1 .55 (5, 6H).
  • 3
  • [ 57625-74-8 ]
  • [ 1191-17-9 ]
  • [ 84542-11-0 ]
YieldReaction ConditionsOperation in experiment
0.1 g To a solution of intermediate 39c (1 .0 g, 1 .0 eq) in DOM (30 mL) at 0 00 Ti014 (5.3 g, 5.0 eq) was added and stirred at room temperature for 30 mm. Then, dichloromethylmethyl ether (3.22 g, 5.0 eq) was added under cooling and stirred at room temperature over night. The reaction mixture was quenched with 1 N HCI (pH=3) andextracted with ethyl acetate, washed with water and dried. The product was obtained by concentrating under vacuo. The product was purified by combiflash to yield the title compound (0.1 g) as a colourless liquid. 1H NMR: (ODd3, 300MHz) 6 9.93(d, 4H) 7.77-7.80 (d, 2H), 7.42-7.45 (d, 1 H), 3.60 (5, 3H), 1 .55 (5, 6H).
 

Historical Records