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Chemical Structure| 51814-17-6 Chemical Structure| 51814-17-6

Structure of 51814-17-6

Chemical Structure| 51814-17-6

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Product Details of [ 51814-17-6 ]

CAS No. :51814-17-6
Formula : C17H23NO6
M.W : 337.37
SMILES Code : O=C(OCC)CCN(C(OCC1=CC=CC=C1)=O)CC(OCC)=O
MDL No. :MFCD16620779

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Application In Synthesis of [ 51814-17-6 ]

* 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 [ 51814-17-6 ]

[ 51814-17-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 51814-17-6 ]
  • [ 51814-19-8 ]
YieldReaction ConditionsOperation in experiment
72% Reference Example 63 Ethyl 1-benzyloxycarbonyl-4-oxopyrrolidine-3-carboxylate To a solution of ethyl 3-[N-benzyloxycarbonyl-N-(ethoxycarbonyl methyl)amino]ethylpropionate (26.8 g, 79.5 mmol) in ethanol (200 mL), sodium ethoxide (20% solution in ethanol, 40.6 mL, 119.3 mmol) was added, and the mixture was heated under reflux for 2 hours. After concentrating the reaction mixture under reduced pressure, the residue was dissolved in water (100 mL). Concentrated hydrochloric acid was added to this solution in an ice bath for acidification, and the solution was extracted with chloroform (100 mL*3). The extract was washed with saturated aqueous solution of sodium chloride (100 mL), and dried with anhydrous sodium sulfate. After the filtration, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (hexane:ethyl acetate, 2:1) to obtain 16.7 g (72%) of the title compound as a pale brown oily product. 1H-NMR (400 MHz, CDCl3)delta ppm: 1.25-1.33 (3H, m), 3.87-4.37 (7H, m), 5.16-5.22 (2H, m), 7.23-7.41 (5H, m). MS (ESI) m/z: 314 (M+Na)+.
With sodium ethanolate; In tetrahydrofuran; at 25 - 32℃; for 2h; [Reference Example 3] Synthesis of 1-benzyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylate [Show Image]; 0.35 kg of sodium ethoxide (5.15 mol) was suspended in 9.47 L of tetrahydrofuran. While this suspension was stirred, 3.16 L of a tetrahydrofuran solution containing 1. 64 kg of the crude product of ethyl 3-benzyloxycarbonyl-3-(ethoxycarbonylmethylamino)propionate (equivalent to 4.68 mol) was added dropwise at an internal temperature of 25 to 32C. The mixture was then stirred at an internal temperature of 25 to 32C for 2 hours. While the reaction mixture was stirred, 5.15 L of 1 mol/L hydrochloric acid (pH 4.78) was added at an internal temperature of 27 to 28C and the mixture was stirred for 10 minutes (pH changed from 4.78 to 4.76). Subsequently, tetrahydrofuran (approx. 12 L) was evaporated under reduced pressure. To the resulting residue, 7.89 L of ethyl acetate was added and the mixture was stirred for 5 minutes. The reaction mixture was then allowed to stand and the organic layer (top layer) was collected. To this layer, 3.95 L of water was added and the mixture was stirred for 5 minutes. The mixture was allowed to stand again and the organic layer (top layer) was collected. To this layer, 3.95 L of 28% brine was added and the mixture was stirred for 5 minutes. The mixture was allowed to stand again and the organic layer (top layer) was collected. To this layer, 0.39 kg of anhydrous sodium sulfate was added and the mixture was stirred for 1 hour. The resulting solid was separated by filtration and washed with 1.58 L of ethyl acetate. The filtrate and the wash were combined and concentrated under reduced pressure. This product was then dried under reduced pressure at an external temperature of 40C for 30 minutes. The resulting pale brown oil (1.52 kg) was dissolved in 9.47 L of diisopropyl ether and the solution was stirred at an internal temperature of 25C. Once the formation of crystals was observed (internal temperature of 25C), the solution was further stirred for 15 minutes at an internal temperature of 25 to 28C. Subsequently, the solution was cooled in an ice bath under stirring and was kept stirred for 30 minutes at an internal temperature of 10C or below. The crystals were then collected by filtration at an internal temperature of 7 C and washed with a chilled, 4: mixtures of diisopropyl ether/hexane (3.95 L, internal temperature of 3C). The washed crystals were drained for 15 minutes and air-dried overnight. Subsequently, the product was dried under reduced pressure at 40C for 9 hours. This gave 1.03 kg of the title compound as a faintly yellowish white powder (75% yield in the two steps). Melting Point: 56.6-59.7C EI-MS : m/z 91 (base peak), 291 (M)+
With sodium methylate; In toluene; at -5 - 25℃; 5 ~ 10 780ml toluene was added to 3000ml reaction flask, was added 36.2g sodium methoxide,After stirring for 5 minutes, the temperature was lowered to -5 to 0 C, a solution of 480 ml of a toluene solution of the compound represented by the formula 4-1 was added dropwise,After the dropwise temperature was raised to 20-25 C and stirred for 2-3 hours, TLC (thin layer chromatography) showed that the reaction was completed and added,Add water 400ml, concentrated hydrochloric acid was added dropwise at 20 ~ 25 , adjusted pH3-4, stirred for 30 minutes, the pH was measured in the 3-4;The organic layer was separated, concentrated under reduced pressure at 60-65 C, concentrated and dried, then added with anhydrous ethanol l60-65 C with toluene,With two, each 120ml, evaporated to give after the oil that compound of Formula 3, the reaction is as follows
 

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