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Chemical Structure| 110706-49-5 Chemical Structure| 110706-49-5

Structure of 110706-49-5

Chemical Structure| 110706-49-5

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Product Details of [ 110706-49-5 ]

CAS No. :110706-49-5
Formula : C8H9ClO2
M.W : 172.61
SMILES Code : ClC1=CC=C(CO)C(CO)=C1
MDL No. :MFCD15147234

Safety of [ 110706-49-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 110706-49-5 ]

* 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 [ 110706-49-5 ]

[ 110706-49-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 54109-03-4 ]
  • [ 110706-49-5 ]
YieldReaction ConditionsOperation in experiment
83% With phenylsilane; potassium hydroxide; In tetrahydrofuran; for 4h;Schlenk technique; Inert atmosphere; Reflux; General procedure: Isobenzofuran-1(3H)-one (0.4 mmol), KOH (0.4 mmol), PhSiH3 (1.2 mmol), dried THF (2 mL) were charged in a Schlenk tube(15 mL) under N2 atmosphere. The mixture was refluxed for 4 h. After cooling to rt, the reaction was quenched with EtOH(0.5-1 mL). Solvent was removed under reduced pressure and the crude residue was purified by column chromatography on silica gel with petroleum ether-ethyl acetate as the eluent to afford the desired product.
  • 2
  • [ 118-45-6 ]
  • [ 54109-03-4 ]
  • [ 110706-49-5 ]
  • 3
  • [ 110706-49-5 ]
  • [ 54109-03-4 ]
  • [ 19641-29-3 ]
  • 4
  • [ 89-20-3 ]
  • [ 110706-49-5 ]
YieldReaction ConditionsOperation in experiment
Step 2; A solution of the previous acid (802.9 mg, 4 mmol) in tetrahydrofuran was added to a cooled (-75 C) slurry of lithium aluminum hydride, 95% (320.6 mg, 8 mmol) in tetrahydrofuran over 25 min. period. The reaction mixture was allowed to warm up to room temperature then heated to reflux for 18 hours. The reaction mixture was quenched with water, 15% sodium hydroxide, and water in ice bath. The separated organic layer was dried to yield 607.8 milligrams of 4-chlorobenzen-1,2-dimethanol.
  • 5
  • [ 89-20-3 ]
  • [ 110706-49-5 ]
  • [ 110706-48-4 ]
YieldReaction ConditionsOperation in experiment
EXAMPLE X5 1,2-Bishydroxymethyl-4-chlorobenzene The title compound was prepared from 25 g (124.6 mmole) of <strong>[89-20-3]4-chlorophthalic acid</strong> by an analogous procedure to that described in Example X2. 1 H-nmr delta (CDCl3): 7.4-7.1(3H,m); 4.57(2H,broad m, exchanges with D2 O); 4.50(4H,s).
 

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