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Chemical Structure| 897043-85-5 Chemical Structure| 897043-85-5

Structure of 897043-85-5

Chemical Structure| 897043-85-5

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Product Details of [ 897043-85-5 ]

CAS No. :897043-85-5
Formula : C13H21NO5
M.W : 271.31
SMILES Code : O=C(C1(C)CN(C(OC(C)(C)C)=O)CC1=O)OCC
MDL No. :MFCD17012785
InChI Key :YDASEKAEWNKGEJ-UHFFFAOYSA-N
Pubchem ID :16753421

Safety of [ 897043-85-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 897043-85-5 ]

* 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 [ 897043-85-5 ]

[ 897043-85-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 146256-98-6 ]
  • [ 74-88-4 ]
  • [ 897043-85-5 ]
YieldReaction ConditionsOperation in experiment
63% With 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; at 20℃; for 1.25h; To 4-oxo-pyrrolidine-1 ,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (1.02 g, 4.0 mmol) in THF at rt was added DBU (4.1 mmol). After 15 min, iodomethane (4.0 mmol) was added and the resultant mixture was stirred for 1 h. The mixture was concentrated and the resultant slurry was partitioned between chloroform and water. The aqueous portion was extracted twice and the combined organic solutions were dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (4:1 hexanes/ethyl acetate) provided 677 mg (63percent) of the title compound as a colorless oil.
58.1% With potassium carbonate; In acetone; at 0 - 20℃; for 3.96667h; To a stirring solution of 1a (43.53 g, 169.2 mmol) dissolved inanhydrous acetone (846 mL) was added potassium carbonate(70.14 g, 507.6 mmol). Iodomethane (21.08 mL, 338.4 mmol) wasadded dropwise at 0 C for about 28 min. After the addition wascomplete, the reaction mixturewas stirred at the same temperaturefor 0.5 h and then allowed to stir for another 3 h at room temperature,and then filtered. The filtrate was concentrated under reducepressure at below 35 C to give a yellow oil. The residue was dissolvedwith dichloromethane (600 mL), and washed with water(100 mL 3), brine (80 mL 2), dried over anhydrous sodiumsulfate, and evaporated under vacuo. The residue was purified bycolumn chromatography (silica gel) eluted with petroleum etherand ethyl acetate (v: v 5: 1) to afford the title compound 1b(26.67 g, 58.1percent) as a pale yellow oil. 1H NMR (400 MHz, CDCl3)d (ppm): 4.28 (d, J 11.8 Hz, 1H), 4.19 (qd, J 7.1, 1.5 Hz, 2H), 4.05 (t,J 19.7 Hz, 1H), 3.81 (d, J 19.4 Hz, 1H), 3.47 (d, J 11.8 Hz, 1H),1.49 (s, 9H), 1.41 (s, 3H), 1.25 (t, J 7.1 Hz, 3H). MS-ESI (m/z): 289.13(M NH4).
32 g With potassium carbonate; In acetone; at 26℃; for 16h; To a solution of Intermediate 12 (50 g, 194.5 mmol) in acetone (500 mL), K2CO3 (53.6 g, 389.1 mmol) and methyl iodide (55.2 g, 389.1 mmol) were added slowly and stirred at 26 °C for 16 h. On completion, reaction mixture was filtered through celite and the filtrate was concentrated and purified by silica gel (100-200 mesh) columnchromatography (0-10percent EtOAc in petroleum ether as eluent) to afford Intermediate 13 (32 g, 60 percent Yield, pale yellow liquid).JH NMR (400MHz, CDCb) delta 4.27 (br d, J = 11.7 Hz, 1H), 4.19 (dq, J = 1.7, 7.1 Hz, 2H), 4.14-3.96 (m, 1H), 3.81 (d, J = 19.6 Hz, 1H), 3.46 (br d, J = 11.7 Hz, 1H), 1.49 (s, 9H), 1.41 (s, 3H), 1.29-1.22 (m, 3H).
 

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