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Chemical Structure| 212890-86-3 Chemical Structure| 212890-86-3

Structure of 212890-86-3

Chemical Structure| 212890-86-3

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Product Details of [ 212890-86-3 ]

CAS No. :212890-86-3
Formula : C12H23NO3
M.W : 229.32
SMILES Code : CC1(C)C[C@@H](CO)N(C(OC(C)(C)C)=O)C1
MDL No. :MFCD18711410

Safety of [ 212890-86-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 212890-86-3 ]

* 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 [ 212890-86-3 ]

[ 212890-86-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1001353-87-2 ]
  • [ 212890-86-3 ]
YieldReaction ConditionsOperation in experiment
75% With borane-THF; In tetrahydrofuran; at 0℃; for 3h;Inert atmosphere; Compound 10-3 (1.13 g, 4.66 mmol) was dissolved in THF (10 mL) and borane (10mL, 1 M in THF) was slowly added dropwise to the reaction flask under nitrogen at 0 C. . After the reaction was completed, the reaction was quenched with methanol (10 mL).The reaction solution was concentrated and purified by column chromatography (eluent: PE/ EtOAc (v / v) = 3/2) to give 0.8 g of a colorless oil Rate: 75%.
With borane-THF; In tetrahydrofuran; at 0 - 20℃; Step 1: Into a 250-mL 3-necked round-bottom flask, was placed (2S)-1-(tert-butoxycarbonyl)- 4,4-dimethylpyrrolidine-2-carboxylic acid (3.9 g, 16.03 mmol, 1.00 equiv), and THF (50.00 mL). This was followed by the addition of BTb-THF (48.06 mL, 48.07 mmol, 3.00 equiv) dropwise with stirring at 0 ?C. The resulting solution was stirred for overnight at room temperature. The reaction was then quenched by the addition of 50 mL of MeOH. The reaction mixture was then heated to reflux for 3 h. The reaction mixture was cooled to room temperature. The resulting mixture was concentrated. The resulting solution was extracted with 3x100 mL of dichloromethane dried over anhydrous sodium sulfate and concentrated. This resulted in tert-butyl (2S)-2-(hydroxymethyl)-4,4-dimethylpyrrolidine-1-carboxylate.
 

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