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Chemical Structure| 660416-37-5 Chemical Structure| 660416-37-5
Chemical Structure| 660416-37-5

Methyl 3-Fluoro-5-(hydroxymethyl)benzoate

CAS No.: 660416-37-5

4.5 *For Research Use Only !

Cat. No.: A476879 Purity: 98+%

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Product Details of [ 660416-37-5 ]

CAS No. :660416-37-5
Formula : C9H9FO3
M.W : 184.16
SMILES Code : O=C(OC)C1=CC(CO)=CC(F)=C1
MDL No. :MFCD23709601

Safety of [ 660416-37-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 660416-37-5 ]

* 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 [ 660416-37-5 ]

[ 660416-37-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 17449-48-8 ]
  • [ 660416-37-5 ]
YieldReaction ConditionsOperation in experiment
57% 5-Fluoroisophthalic acid dimethylester (1.6 g, 7.54 mmol) (J. Org. Chem ; 1969,34, 1960-1961) WAS dissolved in tetrahydrofuran (15 ml). Thereafter, therein 2.0 M lithiumborohydride tetrahydrofuran solution (2.6 ml, 5.27 mmol) was slowly added dropwise at 0C, and the reaction mixture was refluxed for 3 hours. The reaction mixture was acidified with IN HC1 aqueous solution, concentrated under reduced pressure to remove solvent, and extracted with chloroform. Combined organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography (dichloromethane: METHANOL = 99 : 1), to give 800 mg (yield: 57%, white solid) of the target compound. 1H NMR (400MHZ, CDCl3) : 63. 92 (D, J=1. 6Hz, 3H), 4.75 (d, J=4Hz, 2H), 7.29-7. 32 (m, 1H), 7.61 (dd, J=9. 2, 1. 6Hz, 1H), 7.8 (d, J=0. 8Hz, 1H)
50% Method 51; 3-Fluoro-5-hvdroxymethyl-benzoic acid methyl ester; A solution of <strong>[17449-48-8]5-fluoroisophthalic acid dimethyl ester</strong> (Method 50; 301 mg, 1.42 mmol) in THF (15 ml) at 0 C was treated with lithium aluminium hydride (30 mg, 0.7 mmol). The reaction mixture stirred at 25 0C for 2 h. The reaction mixture was quenched with H2O and extracted with EtOAc. The organics were washed with NaCl(sat) and dried with Na2SO4(s) and then concentrated under reduced pressure. The residue was purified by column chromatography utilizing an ISCO system (hexane-EtOAc) to give (120 mg, 50%) of a colourless oil. NMR: 780 (s, IH), 7.62 (d, IH), 7.31 (d, IH), 4.76 (s, 2H), 3.95 (s, 3H), 1.85 (s, br, lH).
 

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