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Chemical Structure| 1024038-25-2 Chemical Structure| 1024038-25-2

Structure of 1024038-25-2

Chemical Structure| 1024038-25-2

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Product Details of [ 1024038-25-2 ]

CAS No. :1024038-25-2
Formula : C13H23NO5
M.W : 273.33
SMILES Code : O=C(N1C[C@H](OCC(OCC)=O)CC1)OC(C)(C)C

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Application In Synthesis of [ 1024038-25-2 ]

* 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 [ 1024038-25-2 ]

[ 1024038-25-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 109431-87-0 ]
  • [ 105-36-2 ]
  • [ 1024038-25-2 ]
YieldReaction ConditionsOperation in experiment
28% the tert-butyl (3R)-3-(ethoxycarbonylmethoxy)pyrrolidine-1-carboxylate used as starting material was prepared as described below A solution of sodium bis(trimethylsilyl)amide in THF (58.7 mL, 58.75 mmol) was added dropwise to a stirred solution of <strong>[109431-87-0](R)-tert-butyl 3-hydroxypyrrolidine-1-carboxylate</strong> (10 g, 53.41 mmol) in DMF (100 mL) over a period of 10 minutes under nitrogen. The resulting solution was stirred at ambient temperature for 10 minutes. Ethyl bromoacetate (8.92 g, 53.41 mmol) was added dropwise over 10 minutes (exotherm. Temperature kept below 30 C. using a cold water bath) and the reaction was stirred at ambient temperature for 20 hours.The reaction mixture was evaporated, EtOAc (200 mL) added and washed sequentially with water (4×50 mL), and saturated brine (50 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product (14 g) as an orange oil.The crude product was purified by flash silica chromatography, elution gradient 20 to 50% EtOAc in isohexane. Pure fractions were evaporated to dryness to afford the product (4.0 g, 28%) as a pale yellow oil.1H NMR (400.13 MHz, DMSO-d6) δ 1.21 (3H, t), 1.41 (9H, s), 1.83-2.01 (2H, m), 3.2-3.32 (4H, m), 4.12 (2H, s), 4.1-4.2 (5H, m)
6.6 g With sodium hydroxide; In tetrahydrofuran;Cooling with ice; A solution of tert-butyl (3R)-3-hydroxypyrrolidine-1-carboxylate (7.0 g) in THF (30 mL) was added to a suspension of 60% sodium hydroxide (2.3 g) in THF (40 mL) under ice-cooling. At the same temperature, a THF (30 mL) solution of ethyl bromoacetate (13 mL) was added to the mixture, and the mixture was stirred overnight. After water and EtOAc were added to the reaction mixture, extraction thereof was performed using EtOAc, and the extract was washed with saturated brine. The organic layer was dried over MgSO4 and filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Hex:EtOAc = 99:1 to 70:30), whereby tert-butyl (3R)-3-(2-ethoxy-2-oxoethoxy)pyrrolidine-1-carboxylate (6.6 g) was obtained as an oil.
  • 2
  • [ 623-73-4 ]
  • [ 109431-87-0 ]
  • [ 1024038-25-2 ]
YieldReaction ConditionsOperation in experiment
83% With dirhodium tetraacetate; In dichloromethane; at 20℃; for 12h;Inert atmosphere; To a solution of tert-butyl (3R)-3-hydroxypyrrolidine-1-carboxylate (10.0 g, 53.4 mmol, CAS 109431-87-0) and Rh2(OAc)4 (472 mg, 1.07 mmol) in DCM (200 mL) was added a solution of ethyl 2-diazoacetate (12.2 g, 107 mmol) in DCM (100 mL) dropwise. Then the reaction mixture was stirred at 20 C for 12 hrs. On completion, the mixture was diluted with water (200 mL), and extracted with DCM (2 X 100 mL). The organic layer was washed with brine (2 x 100 mL), then concentrated in vacuo. The residue was purified by silica gel chromatography (SiO2) to give the title compound (12.1 g, 83% yield) as yellowish oil.1H NMR (400 MHz, CDCl3) d 4.28 - 4.08 (m, 5H), 3.54 - 3.46 (m, 4H), 2.12 - 2.04 (m, 1H), 1.99 - 1.88 (m, 1H), 1.45 (s, 9H), 1.29 (t, J = 7.2 Hz, 3H).
 

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