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Chemical Structure| 908244-98-4 Chemical Structure| 908244-98-4

Structure of 908244-98-4

Chemical Structure| 908244-98-4

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Product Details of [ 908244-98-4 ]

CAS No. :908244-98-4
Formula : C8H15NO2
M.W : 157.21
SMILES Code : O=C(C1CNCCC1C)OC
MDL No. :MFCD10688310

Safety of [ 908244-98-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 908244-98-4 ]

* 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 [ 908244-98-4 ]

[ 908244-98-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 33402-75-4 ]
  • [ 908244-98-4 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride; hydrogen;1% Pd/C; In methanol; water; at 80℃; under 3102.97 Torr; for 16h;Inert atmosphere; Collection A: Preparation of 4-Me-102A 400-mL Fisher-Porter reactor was charged with methanol (115 mL), concentrated hydrochloric acid (4.8 g), 10% Pd/C (1.5 g) and 4-Me-101 (10.9 g, 42.8 mmol). The mixture was heated to 80 C. and placed under 60 psi hydrogen pressure. The mixture was then stirred for 16 h under these conditions. The mixture was cooled and filtered through a bed of diatomaceous earth. The filtrate was evaporated under reduced pressure to give 4-Me-102 (9.6 g, quantitative). The 1H NMR spectrum was consistent with the assigned structure.
With hydrogen; acetic acid;platinum(IV) oxide; at 45℃; for 16h;Inert atmosphere; To a solution of 32.2 (1.0 eq) in AcOH(25 eq), Pt02 (0.2 eq) was carefully added at rt under N2. Then N2 was changed with H2 and the reaction was stirred at 45 C for 16 h. After the reaction was completed, the mixture was filtered through celite. The organic layer was concentrated to give the target compound (60% yield). The crude product 32.3 was used directly in the next step without purification. ESI-MS (M+H+): 158.2. .H NMR (400 MHz, CDC13) delta: 3.61 (s, 3H), 3.10-3.05 (m, 1H), 2.96-2.92 (m, 1H), 2.79- 2.74 (m, 1H), 2.60-2.51 (m, 1H), 2.48-2.44 (m, 1H), 2.19-2.13 (m, 1H), 1.96-1.93 (m, 1H), 1.47- 1.44 (m, 1H), 0.89 (d, J= 7.2 Hz, 3H).
52 g With platinum(IV) oxide; hydrogen; In acetic acid; at 50℃; for 168h; A hydrogenation flask was charged with AcOH (500 mL) and then Pt02 (15.02 g, 66.2 mmol) was added. Intermediate 1 (50 g, 330.8 mmol) was added and the mixture was hydrogenated at 50 C for 7 days. The RM was filtered over dicalite and the filtrate was evaporated to yield intermediate 2 (52 g), which was used in the next step without further purification.
52 g With platinum(IV) oxide; hydrogen; acetic acid; at 50℃; for 168h; Procedure a: A hydrogenation flask was charged with AcOH (500 mL) and then Pt02 (15.02 g, 66.2 mmol) was added. Intermediate 1 (50 g, 330.8 mmol) was added and the mixture was hydrogenated at 50 C for 7 days. The RM was filtered over dicalite and the filtrate was evaporated to yield intermediate 2 (52 g), which was used in the next step without further purification.
With platinum(IV) oxide; hydrogen; acetic acid; at 50℃; for 168h; Procedure a: A hydrogenation flask was charged with AcOH (500 mL) and then Pt02 (15.02 g, 66.2 mmol) was added. Intermediate 1 (50 g, 330.8 mmol) was added and the mixture was hydrogenated at 50 C for 7 days. The RM was filtered over dicalite and the filtrate was evaporated to yield intermediate 2 (52 g), which was used in the next step without further purification.
52 g With platinum(IV) oxide; hydrogen; acetic acid; at 50℃; for 168h; A hydrogenation flask was charged with AcOH (500 mL) and then Pt02 (15.02 g, 66.2 mmol) was added. Intermediate 1 (50 g, 330.8 mmol) was added and the mixture was hydrogenated at 50 C for 7 days. The RIVI was filtered over dicalite and the filtrate was evaporated to yield intermediate 2 (52 g), which was used in the next step without further purification.

 

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