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Chemical Structure| 931-15-7 Chemical Structure| 931-15-7

Structure of 931-15-7

Chemical Structure| 931-15-7

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Product Details of [ 931-15-7 ]

CAS No. :931-15-7
Formula : C6H13NO
M.W : 115.17
SMILES Code : O[C@H]1[C@@H](N)CCCC1
MDL No. :MFCD09260379

Safety of [ 931-15-7 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314-H317-H410
Precautionary Statements:P264-P270-P271-P272-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:9
UN#:3077
Packing Group:

Application In Synthesis of [ 931-15-7 ]

* 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 [ 931-15-7 ]

[ 931-15-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 24424-99-5 ]
  • [ 931-15-7 ]
  • [ 121282-70-0 ]
YieldReaction ConditionsOperation in experiment
96.29% With triethylamine; In dichloromethane; at 0 - 25℃; for 16h; To a solution of compound 1 (10.00 g, 86.83 mmol) and di-tert-butyl dicarbonate (20.85 g, 95.51 mmol, 21.95 mL) in DCM (100.00 mL) was added TEA (26.36 g, 260.49 mmol, 36.11 mL) at 0 C. The mixture was stirred at 25 C for 16 hr. TLC showed the reaction was completed. The resulting mixture was diluted with DCM (100 mL) and washed with water (60 mL*3). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated to afford the crude. The crude was purified by column (Petroleum ether: Ethyl acetate = 25:1, 10:1, 5:1). Compound 2 (18.00 g, 96.29% yield) was obtained as a white solid. ?H NIVIR (400 IVIHz, CHLOROFORM-d): = 4.69 - 4.18 (m, 1H), 3.22 (br d, J=5.7 Hz, 2H), 2.05 - 1.82 (m, 2H), 1.71 - 1.58 (m, 2H), 1.38 (s, 9H), 1.30 - 0.97 (m, 4H). TLC (Petroleum ether: Ethyl acetate =3:1) Rf= 0.23.
With triethylamine; at 0 - 20℃;Large scale; Deprotection was carried out in 4 batches and a total of 8262.0 g (96.1 %) was isolated. The following yields and purities were obtained for each batch: j0114j 20% Palladium hydroxide (201.7 g) was charged to a pressure vessel as a slurry in MeOH (2 L). Stage 3 (2017 g) was then charged as a solution in MeOH (13 L). The mixture was stirred under H2 (40 psi) at room temperature until TLC (thin layer chromatography) analysis indicated complete consumption of the starting material. The mixture was filtered through an in-line filter and the vessel was washed with MeOH (6 L). The filtrates were transferred to a 50 L vessel and cooled to 0 C. Triethylamine (1371 mL) was added, followed by di-t-butyl dicarbonate (2256 mL), keeping the internal temperature <15 C. When the addition was complete the mixture was stirred at room temperature until TLC indicated complete consumption of the amine intermediate. The reaction mixture was evaporated and the resulting off-white solid was dissolved in DCM (16 L). The solution was washed with H20 (2 x 8 L) and brine (8 L), dried over anhydrous Na2504, filtered, evaporated and dried in a vacuum oven at 40 C.
  • 2
  • [ 121282-70-0 ]
  • [ 931-15-7 ]
  • 3
  • [ 34619-03-9 ]
  • [ 931-15-7 ]
  • [ 121282-70-0 ]
 

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