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Chemical Structure| 84541-46-8 Chemical Structure| 84541-46-8

Structure of 84541-46-8

Chemical Structure| 84541-46-8

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Product Details of [ 84541-46-8 ]

CAS No. :84541-46-8
Formula : C14H13Cl
M.W : 216.71
SMILES Code : CC1=C(CCl)C=CC=C1C2=CC=CC=C2
MDL No. :MFCD03208964

Safety of [ 84541-46-8 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314
Precautionary Statements:P264-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P403+P233-P501
Class:8
UN#:3261
Packing Group:

Application In Synthesis of [ 84541-46-8 ]

* 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 [ 84541-46-8 ]

[ 84541-46-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 84541-46-8 ]
  • [ 76350-90-8 ]
YieldReaction ConditionsOperation in experiment
91% With tetrabutylammomium bromide; water; sodium acetate; at 100℃; for 15h; In four flask 65.0g2- methyl-3-chloromethyl-biphenyl (MCMBP), 2.9g tetra-n-butylammonium bromide, 73.8g50% aqueous solution of sodium acetate, heated to reflux, 100 incubated for 15 hours. after the gas-phase testing of raw materials is less than 1%, the reaction solution was slowly dropped 44.0g30% aqueous NaOH, pH control between 12-13, 100 for 10 hours, 60 standing layered liquor recovered apply The organic layer was mixed with toluene and heptane recrystallized BFA wet product. The crude product was vacuum dried to obtain the final product BFA54.1g, purity greater than 99.5% (GC), a yield of 91.0%.
  • 2
  • [ 76350-90-8 ]
  • [ 84541-46-8 ]
YieldReaction ConditionsOperation in experiment
87% With thionyl chloride; In acetonitrile; To a solution of (2-methyl-[1,1'-biphenyl]-3-yl)methanol (1 g, 5.04 mmol) dissolved in 25 mL acetonitrile in a 50 mL reaction flask was added slowly thionyl chloride (10 mL). The reaction was stirred overnight, and monitored by Thin-Layer Chromatography until the reaction was over, and the poured into water (100 mL). The water phase was extracted with ethyl acetate (2*50 mL), the organic phase were washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and then concentrated under reduced pressure. the residual was purified by column chromatography on silica gel (eluent: ethyl acetate:petroleum ether=1:10; silica gel: 100-140 mesh, Qingdao Marine Chemical Co., Ltd.) to get pure 3-(chloromethyl)-2-methyl-1,1'-biphenyl (0.95 g) with yield of 87%.
77% With thionyl chloride; at 20℃; Add 20 g of biphenyl alcohol (1) to 100 mL of SOCl2,The reaction was carried out overnight at room temperature, and the reaction was monitored by TLC.After the reaction is completed, the SOCl2 is evaporated to dryness.The liquid was allowed to stand for a period of time and then solidified to obtain a white solid, which gave Intermediate 2, yield: 77%.
 

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