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Chemical Structure| 3709-21-5 Chemical Structure| 3709-21-5

Structure of 3709-21-5

Chemical Structure| 3709-21-5

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Product Details of [ 3709-21-5 ]

CAS No. :3709-21-5
Formula : C11H12O4
M.W : 208.21
SMILES Code : O=C(O)C(CCC1=CC=CC=C1)C(O)=O
MDL No. :MFCD01249744

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Application In Synthesis of [ 3709-21-5 ]

* 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 [ 3709-21-5 ]

[ 3709-21-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6628-68-8 ]
  • [ 3709-21-5 ]
YieldReaction ConditionsOperation in experiment
65% With potassium hydroxide; In water; b 2-Phenylethylmalonic Acid A mixture of diethyl 2-phenylethylmalonate (3.61 g) and potassium hydroxide (1.69 g, 2.5 eq) in water (15 ml) was refluxed for 2 h and cooled to room temperature. The solution was washed with diethyl ether (2*10 ml) and then acidified to pH 2 (5M hydrochloric acid). The aqueous phase was extracted with diethyl ether (2*20 ml). The combined extracts were washed with water (2*20 ml), saturated brine (20 ml), dried (MgSO4) and evaporated to give the title compound as a white solid (1.85 g, 65%); νmax (KBr) 3080(br), 1705 cm-1; δH [(CD3)2 CO], 2.18 (2H, m, CH2), 2.70 (2H, m, CH2), 3.40 (1H, t, J 7.4 Hz, CH), 7.25 (5H, m, Ph). DCIMS MNH4+
With potassium hydroxide; In ethanol; at 0 - 20℃; for 24h; General procedure: Sodium (1.0 equiv) is slowly added and dissolved in abs. ethanol (1.4mL/mmol). Then, diethyl malonate (1.0 equiv) is added dropwise and the resulting mixture is stirred during 30 min at room temperature. Then, the respective bromide is added dropwise at room temperature and the resulting mixture is refluxed during 24 h. After removal of volatiles, H2O is added and extractions with Et2O (×3) are performed. The combined organic layers are dried with Na2SO4 and evaporated to afford the crude product which is assumed to contain only the target monoalkylated diethyl ester of type 6. The residue is dissolved in EtOH (0.5 mL/mmol of 6) and cooled at 0C. At the same temperature, a solution of KOH (2.0 equiv) in EtOH (1.5 mL/mmol of 6) is slowly added. The mixture is stirred at rt and the progress of the reaction is followed by TLC, until diethylester 6 is fully consumed (if needed, up to 1.0 equiv of KOH is gradually added). Typically, reaction time is 24h. The mixture is concentrated and the residue is diluted H2O and Et2O. The aqueous phase is separated, washed with Et2O (×2), acidified with HCl 2M to pH ~1 and extracted with AcOEt (×3). The combined organic layers are dried over Na2SO4 and evaporated to afford diacid of type 7. The latter is dissolved/suspended to ΑcOEt (1.8 mL/mmol of 7) and Et2NH (1.2 equiv) is added slowly at 0 C. The temperature is raised at rt, ΗCHO (1.4 equiv) is added and the mixture is refluxed for 4 h. Then, the mixture is concentrated, treated with aq. NaHCO3 5% and washed with Et2O (×3). The aqueous phase is acidified with HCl 2M to pH ~1 and extracted with AcOEt (×3). The combined organic layers are dried over Na2SO4 and evaporated to afford acrylic acid of type 3 inadequately pure form to be used in the P-Michael reaction without further purification.
 

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