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Chemical Structure| 53744-50-6 Chemical Structure| 53744-50-6

Structure of 53744-50-6

Chemical Structure| 53744-50-6

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Product Details of [ 53744-50-6 ]

CAS No. :53744-50-6
Formula : C10H12O3
M.W : 180.20
SMILES Code : OC(C)C1=CC=C(OC(C)=O)C=C1
MDL No. :MFCD01761921

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Application In Synthesis of [ 53744-50-6 ]

* 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 [ 53744-50-6 ]

[ 53744-50-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 13031-43-1 ]
  • [ 53744-50-6 ]
YieldReaction ConditionsOperation in experiment
> 99%Chromat. With borane-ammonia complex; In methanol; water; at 20℃; for 0.0833333h; General procedure: mpg-C3N4/Pd (4 mg) and the ketone or aldehyde (0.35 mmol)were suspended in methanol/water mixture (2 mL, 1:1) in apressure tube. Subsequently, AB (0.75 mmol) was addedand the solution was magnetically stirred for 2 (for aldehydes)or 5 min (for ketones) at room temperature. Aftercompletion of the reaction, the catalyst was filtered andwashed with methanol for further use. The solvent wasremoved under the reduced pressure. The yield of each alcoholwas determined by gas chromatography-mass spectrometry(GC-MS).
1440 g With 5%-palladium/activated carbon; hydrogen; In toluene; at 15 - 20℃; under 6000.6 Torr;Large scale; Put 2880g of toluene, 1440g of p-acetoxyacetophenone (obtained in Example 1), and 72g of Pd / C (50% water content, 5% Pd on dry basis) into a 5L pressure reactor, followed by nitrogen, hydrogen After the replacement, the internal temperature was controlled at 15 to 20 C, and the reaction was stirred under a hydrogen pressure of 8 bar.After the reaction, Pd / C was recovered by filtration, the solvent was recovered by distillation of the filtrate, and the concentrate was further distilled under reduced pressure to obtain 1440 g of 1- (4-acetoxyphenyl) ethanol. The HPLC purity was 99.0%.
  • 2
  • [ 2628-16-2 ]
  • [ 13031-43-1 ]
  • [ 99-93-4 ]
  • [ 53744-50-6 ]
YieldReaction ConditionsOperation in experiment
With acetic anhydride; In palladium-carbon; EXAMPLE 1 This example illustrates the preparation of 4-acetoxystyrene oxide from 4-acetoxystyrene under the invention, the latter compound having been prepared from 4-hydroxyacetophenone (4-HAP) as an intermediate. A solution of 136.2g (1.0 mol) of 4-hydroxyacetophenone and 400 ml of acetic anhydride was heated at reflux for 3 h under a nitrogen atmosphere. The acetic acid and acetic anhydride was distilled overhead in vacuo (30-41C, 2.6 mm Hg). The remaining oil was then distilled in vacuo (132-134C, 2.0 mm Hg) to yield 169.7g (95.2%) of white crystals identified as 4 -acetoxyacetophenone. 4-Acetoxyacetophenone (100.0 g, 0.56 mol) was hydrogenated in a Fluidtron Reactor with 5% Pd/C (3.94 g) at 100 psig. The hydrogenation was carried out at 60C for 5.25 hours. The reactor was depressurized and the catalyst removed via filtration to afford 1-(4--acetoxyphenyl)ethanol as an oil (93.6 g).
 

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