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Chemical Structure| 13752-40-4 Chemical Structure| 13752-40-4

Structure of 13752-40-4

Chemical Structure| 13752-40-4

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Product Details of [ 13752-40-4 ]

CAS No. :13752-40-4
Formula : C16H10
M.W : 202.25
SMILES Code : C#CC1=C2C=CC=CC2=CC3=CC=CC=C13
MDL No. :MFCD00183717
InChI Key :WSZBYXQREMPYLP-UHFFFAOYSA-N
Pubchem ID :4140199

Safety of [ 13752-40-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 13752-40-4 ]

* 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 [ 13752-40-4 ]

[ 13752-40-4 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 13752-40-4 ]
  • [ 784-04-3 ]
YieldReaction ConditionsOperation in experiment
77% With hydrogenchloride; water; copper(l) chloride; In methanol; at 20℃; for 6h;Irradiation; Inert atmosphere; General procedure: A 10 mL reaction vessel with a magnetic stirring bar was equipped with phenylacetylene (1 mmol), CuCl (1 mol%), HCl (0.2 mL, 37 wt %) and methanol (2 mL). The mixture was irradiated with a blue LED (5 W) and stirred under at r.t. in an air atmosphere for 6 h. The distance of the reaction vial from the light is about 2 centimeter. After the reaction, the solvent was removed under reduced pressure. Purification of the crude product was achieved by flash column chromatography using petrol ether/ethyl acetate (6:1~10:1) as eluent.
54% With iron(III) sulfate hydrate; acetic acid; at 95℃; for 24h;Schlenk technique; General procedure: Ferric sulfate hydrate (I, 8 mol%), glacial acetic acid (5 mL) and the alkyne (1 - 2 mmol) were introducedinto a 50 mL Schlenk tube, equipped with an air condenser, and the mixture kept under stirring at 95 C or120 C, until consumption of the substrate or no further conversion, as evidenced by TLC or GC. Uponcooling, the supernatant solution was poored into water and the residue washed twice with diethyl ether.After extraction with diethyl ether ( 2), the combined organic layers were washed with a saturated aqueoussolution of sodium bicarbonate and then water until neutrality. Alternatively, the crude from the reactions ofsubstrates featuring hydroxyl or carbonyl groups, as for 12, 15, 20 and 22, was obtained by removing aceticacid under vacuum, in order to reduce loss of material during biphasic extraction. The products were purified
 

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