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Chemical Structure| 375368-94-8 Chemical Structure| 375368-94-8

Structure of 375368-94-8

Chemical Structure| 375368-94-8

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Product Details of [ 375368-94-8 ]

CAS No. :375368-94-8
Formula : C11H12BrFO2
M.W : 275.11
SMILES Code : O=C(OC(C)(C)C)C1=CC=C(F)C(Br)=C1
MDL No. :MFCD03095011
InChI Key :MUGCZCJMBJFCIX-UHFFFAOYSA-N
Pubchem ID :44754911

Safety of [ 375368-94-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H331
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P310-P330-P361-P403+P233-P405-P501
Class:6.1
UN#:2811
Packing Group:

Application In Synthesis of [ 375368-94-8 ]

* 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 [ 375368-94-8 ]

[ 375368-94-8 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 1007-16-5 ]
  • [ 75-65-0 ]
  • [ 375368-94-8 ]
YieldReaction ConditionsOperation in experiment
Exam ple 1E: Com pound 1OT7Step 1- Add carbonyi diimtcfazoie (3.68 g, 227 mmol) to a mixture of 3-bromo-4-fluoro benzoic acid 1e1 (2.51 g, 115 mmoi) in DMF (25 mL} and stir at RT for about 1 ft. Cool the reaction to CfC and add t-BuOH (5,7 ml, 59,4 mmol). Then add DBU (1.9 mL, 12,8 mmol) dropwise. Allow the mixture to warm to RT and stir for about 21 ft, Dilute the mixture with t-BME and wash successively with 10% titrie acid (aqueous) and saturated NaHCO^ (aqueous). Dry over MgSO4, filter and evaporate the votatiies to obtain 1e2.
  • 2
  • [ 375368-94-8 ]
  • C19H27NO4 [ No CAS ]
  • C30H38BrNO6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In dimethyl sulfoxide; at 50℃; for 18.0h; Step 2: Add anhydrous cesium carbonate (387 mg, 1,13 mmol) to a mixture of 1e2 (310 mg, 1.13 mmol) and 1c2 (255 mg, 0,76 mmol) tn DMSO (4 mL) and stir at S0C for about 18 h. Dilute the mixture t-BME and wash successively with 10% cine acid (aqueous) and saturated NaHCGj (aqueous). Dry over MgSO4, filter and evaporate Ihe volatiles. Purification by flash chromatography (EtOAc/Hexanes) provides 1e3,
  • 3
  • [ 375368-94-8 ]
  • C25H27NO6 [ No CAS ]
  • 4
  • [ 375368-94-8 ]
  • C26H29NO6 [ No CAS ]
  • 5
  • [ 375368-94-8 ]
  • C30H37NO6 [ No CAS ]
  • 6
  • [ 375368-94-8 ]
  • C28H31N3O5 [ No CAS ]
  • 7
  • [ 375368-94-8 ]
  • C27H29N3O5 [ No CAS ]
  • 8
  • [ 375368-94-8 ]
  • C33H36N2O6 [ No CAS ]
YieldReaction ConditionsOperation in experiment
83% With dmap; In tert-butyl alcohol; at 60℃; General procedure: A mixture of benzoic acid (1 eq), di-tert-butyl dicarbonate (3 eq) and DMAP (0.3 eq) were dissolved in tert-butanol and the mixture was stirred at 60 C overnight. The reaction progress was monitored by TLC. Once completed, the solvent was evaporated, and the residue was purified by silica gel column chromatography to give the product.
 

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