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Chemical Structure| 317319-10-1 Chemical Structure| 317319-10-1

Structure of 317319-10-1

Chemical Structure| 317319-10-1

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Product Details of [ 317319-10-1 ]

CAS No. :317319-10-1
Formula : C10H12O4
M.W : 196.20
SMILES Code : O=C(OC)COC1=CC=C(O)C=C1C
MDL No. :MFCD07778439
InChI Key :MKWKLYFKRYJIKT-UHFFFAOYSA-N
Pubchem ID :23549552

Safety of [ 317319-10-1 ]

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 [ 317319-10-1 ]

* 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 [ 317319-10-1 ]

[ 317319-10-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 145691-59-4 ]
  • [ 317319-10-1 ]
  • [ 868835-06-7 ]
YieldReaction ConditionsOperation in experiment
56% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; toluene; at 0 - 20℃; The above benzyl alcohol (0.26 g, 1.0 mmol) and methyl (4-hydroxy-2-methylphenoxy)acetate (0.30 g, 1.5 mmol) and triphenylphosphine (0.50 g, 1.85 mmol) were dissolved in a mixture of anhydrous toluene (3-mL) and tetrahydrofuran (1 mL) and the mixture was cooled to 0° C. Diisopropyl azodicarboxylate (0.22 g, 1.2 mmol) was added dropwise under nitrogen. The reaction mixture was stirred for 12 h at ambient temperature and the solvents were evaporated in vacuo. Column chromatography (silica gel Fluka 60, hexanes/ethyl acetate 98:2-90:10) gave methyl [4-(3,5-dibromo)benzyloxy]-2-methylphenoxy]acetate. Yield: 0.25 g (56percent). RF (SiO2, hexanes/ethyl acetate 8:2) 0.45. 1H NMR spectrum (300 MHz, CDCl3, deltaH): 7.61 (s, 1H); 7.48 (s, 2H); 6.80 (s, 1H); 6.67 (s, 2H); 4.92 (s, 2H); 4.60 (s, 2H); 3.80 (s, 3H); 2.28 (s, 3H).
56% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; toluene; at 0 - 20℃; for 12h; The above benzyl alcohol (0.26 g, 1.0 mmol) and methyl (4-hydroxy-2-methyl- phenoxy) acetate (0.30 g, 1.5 mmol) and triphenylphosphine (0.50 g, 1.85 mmol) were dis- solved in a mixture of anhydrous toluene (3 mL) and tetrahydrofuran (1 mL) and the mixture was cooled to 0 °C. Diisopropyl azodicarboxylate (0.22 g, 1.2 mmol) was added dropwise under nitrogen. The reaction mixture was stirred for 12 h at ambient temperature and the sol- vents were evaporated in vacuo. Column chromatography (silica gel Fluka 60, hexanes/ethyl acetate 98: 2-90:10) gave methyl [4-(3,5-dibromo)benzyloxy]-2-methylphenoxy]acetate. Yield: 0.25 g (56 percent). RF (Si02, hexanes/ethyl acetate 8: 2) 0.45. 1H NMR spectrum (300 MHz, CDCI3, No.H) : 7.61 (s, 1 H) ; 7.48 (s, 2 H) ; 6.80 (s, 1 H) ; 6.67 (s, 2H) ; 4.92 (s, 2 H) ; 4.60 (s, 2 H) ; 3.80 (s, 3 H) ; 2.28 (s, 3 H).
 

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