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Chemical Structure| 215918-39-1 Chemical Structure| 215918-39-1

Structure of 215918-39-1

Chemical Structure| 215918-39-1

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Product Details of [ 215918-39-1 ]

CAS No. :215918-39-1
Formula : C11H21NO4
M.W : 231.29
SMILES Code : O=C(OC(C)(C)C)N1[C@@H](C[C@@H](C1)OC)CO
MDL No. :MFCD30829049

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Application In Synthesis of [ 215918-39-1 ]

* 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 [ 215918-39-1 ]

[ 215918-39-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 215918-38-0 ]
  • [ 215918-39-1 ]
YieldReaction ConditionsOperation in experiment
With lithium borohydride; In tetrahydrofuran; at 0 - 20℃; (2) (2S,4S)-N-Boc-2-(hydroxymethyl)-4-methoxypyrrolidine, INT 32 To a solution of INT 31 (3.10 g, 11.96 mmol) in THF (120 mL) at 0 C. was added lithium borohydride solution (2 M in THF, 11.96 mL, 23.91 mmol). The reaction mixture was stirred at RT overnight. The mixture was cooled to 0 C. and poured onto ice water. The mixture was stirred for 15 min at RT, then extracted with diethyl ether. The aqueous layer was back-extracted with diethyl ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated to afford crude INT 32 as a colorless oil. MS (ESI): [M+H]+ 232.3. 1H NMR (DMSO-d6): δ (ppm) 4.64 (t, 1H), 3.87 (s, 1H), 3.68-3.44 (m, 3H), 3.32-3.26 (m, 1H), 3.21 (s, 3H), 3.18-3.15 (m, 1H), 2.04-1.97 (m, 1H), 1.42-1.34 (m, 1H), 1.40 (s, 9H).
With lithium borohydride; In tetrahydrofuran; at 20℃; (2) (2S,4S)-N-Boc-2-(hydroxymethyl)-4-methoxypyrrolidine, INT 32 To a solution of INT 31 (3.10 g, 1 1 .96 mmol) in THF (120 mL) at 0 C was added lithium borohydride solution (2 M in THF, 1 1.96 mL, 23.91 mmol). The reaction mixture was stirred at RT overnight. The mixture was cooled to 0 C and poured onto ice water. The mixture was stirred for 15 min at RT, then extracted with diethyl ether. The aqueous layer was back-extracted with diethyl ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated to afford crude INT 32 as a colorless oil.MS (ESI): [M+H]+232.3.1H NMR (DMSO-d6): δ (ppm) 4.64 (t, 1 H), 3.87 (s, 1 H), 3.68- 3.44 (m, 3H), 3.32-3.26 (m, 1 H), 3.21 (s, 3H), 3.18-3.15 (m, 1 H), 2.04-1 .97 (m, 1 H), 1.42-1 .34 (m, 1 H), 1 .40 (s, 9H).
With lithium borohydride; In tetrahydrofuran; at 0 - 20℃; To a solution of INT 31 (3.10 g, 11.96 mmol) in THF (120 mL) at 0 C was added lithium borohydride solution (2 M in THF, 11.96 mL, 23.91 mmol). The reaction mixture was stirred at RT overnight. The mixture was cooled to 0 C and poured onto ice water. The mixture was stirred for 15 mm at RT, thenextracted with diethyl ether. The aqueous layer was back-extracted with diethyl ether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and concentrated toafford crude INT 32 as a colorless oil.MS (ESI): [M+H] 232.3. ‘H NMR (DMSO-d6): (ppm) 4.64 (t, 1H), 3.87 (s, 1H), 3.68-3.44 (m, 3H),3.32-3.26 (m, 1H), 3.21 (s, 3H), 3.18-3.15 (m, 1H), 2.04-1.97 (m, 1H), 1.42-1.34 (m, 1H), 1.40 (s, 9H).
 

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