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Chemical Structure| 114990-91-9 Chemical Structure| 114990-91-9

Structure of 114990-91-9

Chemical Structure| 114990-91-9

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Product Details of [ 114990-91-9 ]

CAS No. :114990-91-9
Formula : C7H14O3
M.W : 146.18
SMILES Code : CC(C)(C)C[C@@H](O)C(O)=O
MDL No. :N/A

Safety of [ 114990-91-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H315-H318-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P332+P313-P362-P403+P233-P405-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 114990-91-9 ]

* 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 [ 114990-91-9 ]

[ 114990-91-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 88319-43-1 ]
  • [ 114990-91-9 ]
YieldReaction ConditionsOperation in experiment
54% With sulfuric acid; water; sodium nitrite; at -10 - 20℃; A solution of sodium nitrite (0.801 g, 11.600 mmol) in water (3.75 mL) was added dropwise to a stirred solution of <strong>[88319-43-1](R)-2-amino-4,4-dimethyl-pentanoic acid</strong> (0.843 g, 5.806 mmol) in aqueous sulfuric acid (12 mL, 0.5 M, 6 mmol) at -10 C. The reaction mixture was allowed to slowly attain room temperature overnight. Sodium chloride (1.5 g) was added and the solution was extracted with TBME (4*15 mL). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give the title compound (0.455 g, 54%).
Step 1. 4,4-dimethyl-2(R)-hydroxypentanoic acid <strong>[88319-43-1]4,4-Dimethyl-2(R)-aminopentanoic acid</strong> was converted to 4,4-dimethyl-2(R)-hydroxypentanoic acid using the procedure given in Step 1 of Example 2.
 

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