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Chemical Structure| 138423-86-6 Chemical Structure| 138423-86-6

Structure of 138423-86-6

Chemical Structure| 138423-86-6

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Product Details of [ 138423-86-6 ]

CAS No. :138423-86-6
Formula : C13H23NO4
M.W : 257.33
SMILES Code : O=C(N1[C@H](C(OC)=O)CC(C)(C)C1)OC(C)(C)C
MDL No. :MFCD11040193

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Application In Synthesis of [ 138423-86-6 ]

* 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 [ 138423-86-6 ]

[ 138423-86-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 138423-86-6 ]
  • [ 1001353-87-2 ]
YieldReaction ConditionsOperation in experiment
95% With lithium hydroxide monohydrate; In water; at 0 - 20℃; for 2h;Inert atmosphere; Sealed tube; To a solution of compound 15-2 (4.85 g, 18.86 mmol) in THF (40 mL) was added lithium hydroxide monohydrate aqueous solution (1.5 g, 20 mL) dropwise at 0 C. At the end of the addition, the mixture was stirred at rt for 2.0 hrs. After the reaction was completed, the THF solvent was removed and 50 mL of water was added to the mixture. The resulting mixture was washed with EtOAc (30 mL x 3). The aqueous phase was adjusted to pH 1 with hydrochloric acid (1 M) and extracted with EtOAc (50 mL x 3). The combined organic layers were washed with brine, dried over anhydrous Na2S04 and concentrated in vacuo to give the title compound as a white solid (4.35 g, 95%). The compound was characterized by the following spectroscopic data: MS (ESI, pos.ion) mlz: 244.5 [M+H]+; 'H NMR (400 MHz, CD3OD) δ (ppm): 4.34-4.31 (m, 1H), 3.28-3.22 (m, 1H), 3.20-3.13 (m, 1H), 2.23-2.18 (m, 1H), 1.85-1.80 (m, 1H), 1.46 (s, 9H), 1.01-0.99 (m, 3H), 0.86-0.84 (m, 3H).
95% With lithium hydroxide monohydrate; In tetrahydrofuran; water; at 0 - 20℃; for 2h; Compound 10-2 (4.85 g, 18.86 mmol) was dissolved in THF (40 mL) and an aqueouslithium hydroxide monohydrate solution (1.5 g, 20 mL) was added to the system at 0 C.The mixture was reacted at room temperature for 2.0 hours. After completion of thereaction, THF was removed, water (50 mL) was added and the mixture was washed with EtOAc(30 mL × 3). After partitioning, the aqueous layer was adjusted to pH 1 with dilutehydrochloric acid (1 M) The combined organic phases were washed with saturated brine anddried over anhydrous Na 2SO 4Dried and concentrated to give 4.35 g of white solid, yield:95%.
With water; lithium hydroxide; In ethanol; at 0 - 20℃; for 6h; Example 14, Step dA solution of proline N14c (500 mg, 1.94 mmol) in EtOH (8 mL) was cooled to 0 C, LiOH (93 mg, 3.89 mmol) in water (4 mL) was added, and the reaction mixture was stirred at RT for 6 h. It was then concentrated under reduced pressure, and the resulting crude material was dissolved in water and extracted with Et20 (20 mL). The aqueous phase was acidified to pH 4 with 1 N HC1 and extracted withEtOAc (100 mL). The organic phase was washed with brine, dried over Na2S04 and concentrated in vacuo to afford acid 14d (454 mg). XH NMR (CDC13, δ = 7.26 ppm, 400 MHz): δ 4.42-4.23 (m, 1H), 3.26 (d, J = 10.8, 1H), 3.10 (d, J = 10.8, 1H), 2.30- 2.20 (m, 1H), 1.96-1.82 (m, 1H), 1.50/1.45 (s, 9H), 1.11/1.07 (s, 6H).
 

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