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Chemical Structure| 335013-90-6 Chemical Structure| 335013-90-6

Structure of 335013-90-6

Chemical Structure| 335013-90-6

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Product Details of [ 335013-90-6 ]

CAS No. :335013-90-6
Formula : C9H9ClO3
M.W : 200.62
SMILES Code : O=C(OCC)C1=CC=C(Cl)C(O)=C1
MDL No. :MFCD16250096

Safety of [ 335013-90-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 335013-90-6 ]

* 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 [ 335013-90-6 ]

[ 335013-90-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 64-17-5 ]
  • [ 34113-69-4 ]
  • [ 335013-90-6 ]
YieldReaction ConditionsOperation in experiment
With sulfuric acid; for 16h;Heating / reflux; A solution of 4-chloro-3 -hydroxy-benzoic acid (29.3 mmol) in EtOH (110 rnL) is treated with cone, sulfuric acid (23.6 mL) and heated to reflux for 16h. Water (600 mL), NaHCO3 (100 g) and ether (300 mL) are added successively, the layers are separated and the aqueous layer is extracted twice with ether. The combined organic layers are washed twice with brine, dried over MgSO4 and concentrated in vacuo to give the desired product which is used without further purification. 1H-NMR (CDCl3): δ = 7.73 (s, IH); 7.58 (d, J = 8.3Hz, IH); 7.40 (d, J = 8.3 Hz, IH); 5.87 (s, IH); 4.39 (q, J = 7.0 Hz, 2H); 1.41 (t, J = 7.0 Hz, 3H).
With sulfuric acid; for 16h;Heating / reflux; A solution of 4-chloro-3 -hydroxy-benzoic acid (29.3 mmol) in EtOH (110 mL) is treated with cone, sulfuric acid (23.6 mL) and heated to reflux for 16h. Water (600 mL), NaHCO3 (100 g) and ether (300 mL) are added successively, the layers are separated and the aq. layer is extracted twice with ether. The combined organic layers are washed twice with brine, dried over MgSO4 and concentrated in vacuo to give the desired product which is used without further purification. 1H-NMR (CDCl3): δ = 7.73 (s, IH); 7.58 (d, J = 8.3 Hz, IH); 7.40 (d, J = 8.3 Hz, IH); 5.87 (s, IH); 4.39 (q, J = 7.0 Hz, 2H); 1.41 (t, J = 7.0 Hz, 3H).
 

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