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Chemical Structure| 158020-60-1 Chemical Structure| 158020-60-1

Structure of 158020-60-1

Chemical Structure| 158020-60-1

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Product Details of [ 158020-60-1 ]

CAS No. :158020-60-1
Formula : C9H16N2O3
M.W : 200.24
SMILES Code : CC(OC(N/N=C1COCC/1)=O)(C)C
MDL No. :MFCD28101538

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Application In Synthesis of [ 158020-60-1 ]

* 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 [ 158020-60-1 ]

[ 158020-60-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 22929-52-8 ]
  • [ 870-46-2 ]
  • [ 158020-60-1 ]
YieldReaction ConditionsOperation in experiment
95% In methanol; at 15℃; for 2h; A solution of <strong>[22929-52-8]dihydrofuran-3(2H)-one</strong> (5.0 g, 58 mmol) and tert-butyl hydrazinecarboxylate (7.68 g, 58.08 mmol) in MeOH (50 mL) was stirred at 15° C. for 2 hours. The mixture was concentrated to remove MeOH and afford tert-butyl 2-(dihydrofuran-3(2H)-ylidene)hydrazine-1-carboxylate (11 g, 55 mmol, 95percent yield). 1H NMR (MeOD 400 MHz): delta4.19 (s, 2H), 4.03 (t, J=6.8 Hz, 2H), 2.53 (t, J=7.2 Hz, 2H), 1.50 (s, 9H).
85% In methanol; at 20℃; for 2h; General procedure: A 100 mL 3-neck flask with inert gas valve and septum was charged with (6.50 g, 49.04 mmol) tert-butylhydrazinecarboxylate and 30 mL MeOH. (4.91 g, 49.04 mmol) dihydro-2H-pyran-3(4H)-one was syringed into the flask. The mixture was stirred at rt for 2 h to observe the disappearance of tert-butylhydrazinecarboxylate monitored by LC-MS. The mixture was then dried over Na2SO4 and the solution was filtered and the solvent removed under reduced pressure to yield 10.4 g of white solid (99percent yield). The compound was further purified by passing through a short silica pad using 50percent EtOAc in hexanes.
27.3 g In methanol; at 10 - 35℃; for 12h; (1) Synthesis of t-butyl 2-[dihydrofuran-3(2H)-ylidene]hydrazinecarboxylate 3-oxotetrahydrofuran (10.38 g) was dissolved in methanol (200 mL), and t-butyl carbazate (17.53 g) was added to the solution. The mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated to give the title compound (27.3 g). 1H-NMR (400 MHz, CDCl3) delta (ppm): 1.52 (s, 9H), 2.46 (t, J=6.9 Hz, al), 4.10 (t, J=6.9 Hz, 2H), 4.33 (s, 2H).
1.95 mmol In ethanol;Reflux; To a solution of dihydro(3(2H)-furanone (1 .95 mmol) in ethanol(2 mL) was added tert-butyl carbazate (2.35 mmol) and the reaction was heated to reflux and stirred overnight. Volatiles were removed under reduced pressure to give the titled compound (1.95 mmol) as a white solid. 1H NMR (400 MHz,CDCI3, 3, mixture of isomers): 7.25 (5, 0.75H), 7.12 (5, 0.25 H), 4.34 (t, J= 1.2 Hz, i.5H), 4.24 (t, J=1.2 Hz, 0.5H), 4.12 (t, J = 6.9 Hz, 1 .5H), 4.02 (t, J = 6.9 Hz, 0.5H), 2.78 (td, J = 6.9, 1.2 Hz, 0.5H), 2.48 (td, J = 6.9, 1.2 Hz, 1 .5H), 1.54 (5, 7.5H), 1.53 (5, 1 .5H).

 

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