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Chemical Structure| 1421620-34-9 Chemical Structure| 1421620-34-9

Structure of 1421620-34-9

Chemical Structure| 1421620-34-9

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Product Details of [ 1421620-34-9 ]

CAS No. :1421620-34-9
Formula : C7H3ClF3IO
M.W : 322.45
SMILES Code : FC(F)(OC1=C(C(I)=CC=C1)Cl)F
MDL No. :MFCD30145988

Safety of [ 1421620-34-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1421620-34-9 ]

* 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 [ 1421620-34-9 ]

[ 1421620-34-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 450-96-4 ]
  • [ 1421620-34-9 ]
YieldReaction ConditionsOperation in experiment
To a solution of 1 -chloro-2-(trifluoromethoxy)benzene (2.54 mmol) in 10 mL THF were added 1.42 mL n-BuLi (2.5 M solution in hexane) at -78C. After 40 min, a solution of iodine (2.8 mmol) in 2.5 mL THF was added and stirring was continued at RT overnight. The reaction was quenched with water under cooling and extracted with EtOAc (3x). The combined organic layers were dried over MgS04 and concentrated in vacuo. Purification by CC (KP-SIL from Biotage) using Hept to Hept/EtOAc (4/1 ) gives the desired compound (in a regioisomeric mixture as the major product) as colorless oil. LC-MS (A): tR = 0.99 min; 1H NMR ((CD3)2SO) δ: 7.98 (dd, 1 H), 7.70 (dd, 1 H), 7.21 (t, 1 H).
With n-butyllithium; iodine; In tetrahydrofuran; hexane; A.1.5 Synthesis of 2-chloro-1-iodo-3-(trifluoromethoxy)benzene To a solution of 1-chloro-2-(trifluoromethoxy)benzene (2.54 mmol) in 10 mL THF were added 1.42 mL n-BuLi (2.5 M solution in hexane) at -78 C. After 40 min, a solution of iodine (2.8 mmol) in 2.5 mL THF was added and stirring was continued at RT overnight. The reaction was quenched with water under cooling and extracted with EtOAc (3*). The combined organic layers were dried over MgSO4 and concentrated in vacuo. Purification by CC (KP-SIL from Biotage) using Hept to Hept/EtOAc (4/1) gives the desired compound (in a regioisomeric mixture as the major product) as colorless oil. LC-MS (A): tR=0.99 min; 1H NMR ((CD3)2SO) δ: 7.98 (dd, 1H), 7.70 (dd, 1H), 7.21 (t, 1H).
 

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