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Chemical Structure| 613241-14-8 Chemical Structure| 613241-14-8

Structure of 613241-14-8

Chemical Structure| 613241-14-8

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Product Details of [ 613241-14-8 ]

CAS No. :613241-14-8
Formula : C14H10BrF3
M.W : 315.13
SMILES Code : FC(C1=CC=C(C2=CC=C(CBr)C=C2)C=C1)(F)F
MDL No. :MFCD25460278
InChI Key :KFWJYVSMZTXKKG-UHFFFAOYSA-N
Pubchem ID :22280165

Safety of [ 613241-14-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P261-P280-P305+P351+P338-P310
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 613241-14-8 ]

* 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 [ 613241-14-8 ]

[ 613241-14-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 457889-46-2 ]
  • [ 613241-14-8 ]
YieldReaction ConditionsOperation in experiment
65% With phosphorus tribromide; In diethyl ether; dichloromethane; at 0℃; for 2h; Step B. 4'-Bromomethyl-4-trifluoromethyl-biphenyl; Phosphorous tribromide (8.67mmol, 1.OM in dichloromethane) is added to a stirred solution of 4'-trifluoromethyl-biphenyl-4-yl)-methanol (2.08g, 8.25mmol) in ethyl ether (40mL) at 0 C under inert atmosphere of nitrogen. The reaction is stirred at 0 C for two hours, quenched at 0 C with water, diluted mixture with ethyl acetate, washed with water, then brine. Organics are dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue is purified by column (silica gel) in 0-40% ethyl acetate/hexane gradient to give 1.68g (5.33mmol, 65%) of title compound.
With phosphorus tribromide; The title compound was prepared in the manner analogous to Example 1F using 100F and 1-(bromomethyl)-4-[4-(trifluoromethyl)phenyl]benzene prepared from and phosphorous tribromide and <strong>[457889-46-2](4'-trifluoromethyl-biphenyl-4-yl)-methanol</strong> in a manner analagous to Example 3B. 400 MHz 1H NMR (CDCl3) delta 7.68 (m, 4H), 7.51 (d, 2H), 7.29 (d, 2H), 7.15 (m, 2H), 6.60 (d, 1H), 4.62 (s, 2H), 4.04 (s, 2H), 3.79 (s, 3H), 2.60 (m, 2H), 1.55 (m, 2H), 1.35 (m, 2H), 0.88 (t, 3H).
1.77 g With phosphorus tribromide; In diethyl ether; at 20℃; for 1.5h;Cooling with ice; To an ice cold solution of intermediate M10 (2.02g, lequiv) in anhydrous diethyl ether (20ml) protected with a CaCl2 drying tube to insulate moisture was added phosphorus tribromide (0.38ml, 0.5equiv). The mixture was stirred at room temperature for 1.5h to obtain a clear solution. TLC detection showed that the reaction was complete and then the mixture was quenched with saturated sodium bicarbonate solution. The resulting precipitate was filtered off and the filtrate was extracted with dichloromethane twice (40ml), dried over MgSO4, filtered and then evaporated in vacuo to give intermediate M11 (1.77g) as a white solid which could be used in next step without further purification.
1.77 g With phosphorus tribromide; In diethyl ether; at 20℃; for 1.5h; To an ice cold solution of intermediate Mi0 (2.02 g, 1 equiv) in anhydrous diethyl ether (20 ml) protected with a CaC12 drying tube to insulate moisture was added phosphorus tribromide (0.38 ml, 0.5 equiv). The mixture was stirred at room temperature for 1 .5 h to obtain a clear solution. TLC detection showed that the reaction was complete and then themixture was quenched with saturated sodium bicarbonate solution. The resulting precipitate was filtered off and the filtrate was extracted with dichloromethane twice (40 ml), dried over MgSO4, filtered and then evaporated in vacuo to give intermediate Ml 1 (1.77 g) as a white solid which could be used in next step without further purification.

 

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