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Chemical Structure| 4442-54-0 Chemical Structure| 4442-54-0
Chemical Structure| 4442-54-0

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Product Details of 1,4-Benzodioxane-6-carboxylic acid

CAS No. :4442-54-0
Formula : C9H8O4
M.W : 180.16
SMILES Code : O=C(C1=CC=C(OCCO2)C2=C1)O
MDL No. :MFCD00463509
InChI Key :JWZQJTGQFHIRFQ-UHFFFAOYSA-N
Pubchem ID :2758833

Safety of 1,4-Benzodioxane-6-carboxylic acid

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of 1,4-Benzodioxane-6-carboxylic acid

* 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 [ 4442-54-0 ]

[ 4442-54-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4442-54-0 ]
  • [ 74-88-4 ]
  • [ 143809-21-6 ]
YieldReaction ConditionsOperation in experiment
34% To a round bottom flask equipped with magnetic stirring, an addition funnel and a nitrogen inlet, was added benzo(1,4)dioxan-6-carboxylic acid (18.00 g, 99.91 mmol) and 1,2-dimethoxyethane (667 mL). This mixture was cooled to -75 C. in a dry ice-acetone bath. To this was added 1.3 M sec-butyl lithium in cyclohexane (230.6 mL, 299.7 mmol) over 1 hour, maintaining reaction temperature below -60 C. The reaction was removed from the cooling bath, allowed to warm to -20 C., and subsequently stirred at -20 C. for 45 min. The reaction was cooled to -50 C., and iodomethane (15.6 mL, 249.8 mmol) was added. The reaction was again removed from the cooling bath, allowed to warm to -20 C., and stirred at this temperature for 45 min. All cooling was removed and the reaction stirred at room temperature for 16 hours. The reaction was quenched by addition of a few mls of 1N HCl (aq) and the solvent removed by evaporation. The residue was made substantially acidic by the addition of aqueous 1N HCl. The resultant precipitate was filtered and washed with water to give a light brown solid, 5-methyl-benzo(1,4)dioxan-6-carboxylic acid, (6.60 g, 33.9 mmol) in 34% yield. 1H-NMR (300 MHz, CDCl3) delta (ppm): 7.62 (d, 1H), 6.8 (d, 1H), 4.30 (br s, 4H), 2.52 (s, 3H).
  • 2
  • [ 493-09-4 ]
  • [ 124-38-9 ]
  • [ 4442-53-9 ]
  • [ 4442-54-0 ]
 

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