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Chemical Structure| 2175-91-9 Chemical Structure| 2175-91-9

Structure of 2175-91-9

Chemical Structure| 2175-91-9

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Product Details of [ 2175-91-9 ]

CAS No. :2175-91-9
Formula : C8H10
M.W : 106.17
SMILES Code : CC(C)=C1C=CC=C1
MDL No. :MFCD00011655

Safety of [ 2175-91-9 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H304
Precautionary Statements:P301+P310-P331
Class:3
UN#:3295
Packing Group:

Application In Synthesis of [ 2175-91-9 ]

* 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 [ 2175-91-9 ]

[ 2175-91-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 2175-91-9 ]
  • [ 36321-73-0 ]
  • [ 115695-90-4 ]
  • 2
  • [ 2175-91-9 ]
  • [ 608-21-9 ]
  • [ 942222-16-4 ]
YieldReaction ConditionsOperation in experiment
55% With n-butyllithium; In toluene; at -5 - 20℃; for 2.33333h;Product distribution / selectivity; b) n-Butyllithium variant, from 1.2.3-tribromo-benzene; To a stirred solution of 1,2,3-tribromo-benzene (4.34g, 13.8 mmol) and 6,6-dimethylfulvene (2.38g, assay 92.6%, 20.7 mmol) in dry toluene (60 ml) under a nitrogen atmosphere, 5.5 ml of a 2.5M toluene solution of /j-butyllithium (14.5 mmol) were added dropwise at -5 to O0C within 10 minutes. After a further 10 minutes at O0C and 2 hours at ambient temperature, the reaction mixture was poured onto a saturated aqueous solution of ammonium chloride, extracted with ethyl acetate, washed with brine and water, dried over sodium sulphate and evaporated. Purification of the crude material on silca gel in hexane afforded 2.38g of the desired product as a yellow oil (assay 84% by g.l.c, 55% yield).
With n-butyllithium; In toluene; at -5 - 20℃; for 2.33333h;Inert atmosphere; To a stirred solution of 1 ,2,3-tribromo-benzene (4.34g, 13.8 mmol) and 6,6-dimethylfulvene (2.38 g, assay 92.6%, 20.7 mmol) in dry toluene (60 ml) under a nitrogen atmosphere, 5.5 ml of a 2.5M toluene solution of n-butyllithium (14.5 mmol) were added dropwise at -5 to 0C within 10 minutes. After a further 10 minutes at 0C and 2 hours at ambienttemperature, the reaction mixture was poured onto a saturated aqueous solution of ammonium chloride, extracted with ethyl acetate, washed with brine and water, dried over sodium sulphate and evaporated. Purification of the crude material on silca gel in hexane afforded 2.38 g of the desired product as a yellow oil (assay 84% by g.l.c, 55% yield). This reaction is also disclosed in WO 2007/068417.
 

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