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Chemical Structure| 312325-74-9 Chemical Structure| 312325-74-9

Structure of 312325-74-9

Chemical Structure| 312325-74-9

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Product Details of [ 312325-74-9 ]

CAS No. :312325-74-9
Formula : C7H5BrN2
M.W : 197.03
SMILES Code : N#CCC1=CC(Br)=NC=C1
MDL No. :MFCD11100738
InChI Key :PBNYXTKBDQXJFM-UHFFFAOYSA-N
Pubchem ID :53429026

Safety of [ 312325-74-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 312325-74-9 ]

* 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 [ 312325-74-9 ]

[ 312325-74-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 106-93-4 ]
  • [ 312325-74-9 ]
  • [ 1279815-46-1 ]
YieldReaction ConditionsOperation in experiment
With sodium hydride; In diethyl ether; dimethyl sulfoxide; mineral oil; at 20℃; for 18.0h;Cooling with water bath; A solution of (2-bromo-pyridin-4-yl)-acetonitrile (1.20 g, 6.09 mmol) and the 1,2- dibromoethane (0.663 mL, 7.61 mmol) in a mixture of dry Et20 (5 mL) and dry DMSO (1 mL) is added to a suspension of NaH (60% dispersion in mineral oil, 585 mg, 14.6 mmol) in dry DMSO (10 mL) while controlling the resulting exotherm by cooling in a water bath, and the resulting mixture is stirred at room temperature. After 18 hours, water (10 mL) and ethyl acetate (10 mL) are added, phases are separated and the aqueous layer is extracted with ethyl acetate (3 x 10 mL). The combined organic layers are washed with brine (30 mL) and dried over MgS04, filtered and concentrated. The residue is purified on Si02 eluting with a gradient of 0-60% ethyl acetate in heptane to afford l-(2-bromo-pyridin-4-yl)-cyclopropanecarbonitrile as a solid (ES+ m/z 223.36; 225.39).
With sodium hydride; In diethyl ether; dimethyl sulfoxide; mineral oil; at 20℃; for 18.0h; A solution of (2-bromopyridin-4-yl)-acetonitrile (1.20 g, 6.09 mmol) and the 1,2- dibromoethane (0.663 mL, 7.61 mmol) in a mixture of anhydrous Et20 (5 mL) and anhydrous DMSO (1 mL) is added to a suspension of NaH (60% dispersion in mineral oil, 585 mg, 14.6 mmol) in anhydrous DMSO (10 mL) while controlling the resulting exotherm by cooling in a water bath, and the resulting mixture is stirred at room temperature. After 18 hours, water (10 mL) and EtOAc (10 mL) are added, phases are separated and the aqueous layer is extracted with EtOAc (3 x 10 mL). The combined organic layers are washed with brine (30 mL) and dried over MgS04, filtered and concentrated. The residue is purified by silica gel chromatography eluting with a gradient of 0-60% EtOAc in heptane to afford l-(2-bromopyridin-4-yl)- cyclopropanecarbonitrile as a solid. MS mJz 223 A, 225 A.
 

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