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[ CAS No. 660440-57-3 ] {[proInfo.proName]}

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Chemical Structure| 660440-57-3
Chemical Structure| 660440-57-3
Structure of 660440-57-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 660440-57-3 ]

CAS No. :660440-57-3 MDL No. :MFCD04115652
Formula : C11H15BO4 Boiling Point : -
Linear Structure Formula :- InChI Key :PRCOGZNDLWXGHB-UHFFFAOYSA-N
M.W : 222.05 Pubchem ID :3851700
Synonyms :

Safety of [ 660440-57-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 660440-57-3 ]

* 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 [ 660440-57-3 ]

[ 660440-57-3 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 660440-57-3 ]
  • [ 166316-48-9 ]
YieldReaction ConditionsOperation in experiment
72% With sodium hydroxide for 3h; Heating;
  • 2
  • [ 40640-98-0 ]
  • [ 660440-57-3 ]
  • 3
  • [ 64-17-5 ]
  • [ 166316-48-9 ]
  • [ 660440-57-3 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride for 24h; Heating / reflux; P20 Preparation 20; [4- [2-ETHOXYCARBONYLETHYL] PHENYLBORONIC] acid (P20) 4- (2-Carboxyethyl) phenylboronic acid (4 [G,] 20.6 [MMOL)] was stirred at reflux for 24 hours in [ETHANOLIC] hydrochloric acid. The reaction mixture was cooled, then concentrated to afford the title compound as an oil.
  • 4
  • [ 660440-56-2 ]
  • [ 660440-57-3 ]
  • [ 660440-52-8 ]
YieldReaction ConditionsOperation in experiment
With pyridine; N-ethyl-N,N-diisopropylamine In dichloromethane at 20℃; for 4h; P24 Preparation 24; [3- {4- [3- (4-NITROPHENYL)-2-OXO-2H-PYRIDIN-1-YL] PHENYL) PROPIONIC] acid ethyl ester (P24) [3- (4-NITROPHENYL)-1H-PYRIDIN-2-ONE] (P3) (0.2 [G,] 0.92 [MMOL),] copper [(II)] acetate (0.334 [G,] 2 equiv. ), diisopropylethylamine (0.31 mL, 2 equiv. ), and pyridine (0.15 mL, 2 equiv. ) were added to a stirred solution of 4- (2-ethoxycarbonylethyl) phenyl boronic acid (0.308 g, 1.3 [MMOL)] in dichloromethane (10 mL). The reaction mixture was then stirred under argon at room temperature for 4 hours. The solution was then filtered through celite, concentrated and purified by chromatography on silica gel (50% v/v ethyl acetate in hexane) to afford the title compound as an oil. MS (ES+ve): [M+H] [+] at [M/Z] 393 [(C22H2ON205] requires [M+H] [+ AT M/Z] 393).
  • 5
  • [ 660440-57-3 ]
  • [ 850568-48-8 ]
YieldReaction ConditionsOperation in experiment
70% With diisobutylaluminium hydride In tetrahydrofuran; toluene at -78 - 20℃; Inert atmosphere;
  • 6
  • [ 102854-88-6 ]
  • [ 660440-57-3 ]
  • [ 850568-48-8 ]
YieldReaction ConditionsOperation in experiment
70% In tetrahydrofuran reaction with aluminium hydride at -78 to 0 °C followed by reaction with Rochelle's salt for 12 h at 0 °C to room temp.; one phase-switch purification used;
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