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Chemical Structure| 362706-25-0 Chemical Structure| 362706-25-0

Structure of 362706-25-0

Chemical Structure| 362706-25-0

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Product Details of [ 362706-25-0 ]

CAS No. :362706-25-0
Formula : C10H17NO3
M.W : 199.25
SMILES Code : O=C(N1C(C)CC(C1)=O)OC(C)(C)C
MDL No. :MFCD22376634
InChI Key :ABBMDHUKQONVIE-UHFFFAOYSA-N
Pubchem ID :18379296

Safety of [ 362706-25-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 362706-25-0 ]

* 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 [ 362706-25-0 ]

[ 362706-25-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 23770-07-2 ]
  • [ 24424-99-5 ]
  • [ 362706-25-0 ]
YieldReaction ConditionsOperation in experiment
66.5% With hydrogen;palladium on carbon; In ethanol; under 2068.65 Torr; Step 5: terf-butyl 5-methyl-(pyrrolidin-3-one)-1-carboxylateA solution of <strong>[23770-07-2]1-benzyl-5-methylpyrrolidin-3-one</strong> (2 g, 10.57 mmol), BoC2O (2.77 g, 12.98 mmol) and Pd/C (0.3 g) in EtOH (20 mL) was stirred under H2 (40 psi) overnight. After TLC showed the reaction was complete, the reaction mixture was filtered and the filtrate was concentrated. The residue was purified by column chromatography (9:1 PE/EA) to give terf-butyl 5-methyl-(pyrrolidin-3-one)-1-carboxylate (1.4 g, 66.5%) as colorless oil (1.4 g, 66.5%): 1H NMR (400 MHz, CDCI3) delta ppm 7.33-7.23 (m, 5H), 4.18-4.15 (d, J = 13.2 Hz, 1 H), 3.29-3.14 (m, 1 H), 2.99-2.93 (m, 1 H), 2.65-2.60 (m, 1 H), 2.51-2.45 (m, 1 H), 2.16-2.08 (m, 1 H), 1.34-1.32 (m, 3H); ES-LCMS does not ionize.
54% With hydrogen; In ethyl acetate; (393e) Di tert-butyl dicarbonate (1.45 gm, 6.6 mmol) was added to a solution of <strong>[23770-07-2]1-benzyl-5-methyl-3-pyrrolidinone</strong> (1.13 gm, 6.0 mmol) in ethyl acetate (30 ml) and palladium hydroxide. The reaction was pressured to 50 psi hydrogen and shaken for 18 h. The reaction was filtered, concentrated and purified by flash chromatography to give N-Boc-5-methyl-3-pyrrolidinone (0.87 gm, 54%) as an oil. (393f) Following a procedure analogous to that used in example (357), but using the N-Boc-5-methyl-3-pyrrolidinone from step (393e) and triethyl phosphonoacetate in DMF with sodium hydride, to prepare the a-d unsaturated ester, the title compound (0.058 g. 44%) was prepared as a white amorphous solid, MS (M+H)+=494.
 

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