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Chemical Structure| 856250-87-8 Chemical Structure| 856250-87-8

Structure of 856250-87-8

Chemical Structure| 856250-87-8

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Product Details of [ 856250-87-8 ]

CAS No. :856250-87-8
Formula : C12H15IO2
M.W : 318.15
SMILES Code : O=C(OC(C)(C)C)CC1=CC=C(I)C=C1
MDL No. :MFCD27930096

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Application In Synthesis of [ 856250-87-8 ]

* 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 [ 856250-87-8 ]

[ 856250-87-8 ] Synthesis Path-Downstream   1~3

  • 2
  • [ 1798-06-7 ]
  • [ 36805-97-7 ]
  • [ 856250-87-8 ]
YieldReaction ConditionsOperation in experiment
44% In toluene; at 80℃; for 2h; A solution of 4-iodo phenyl acetic acid (Lancaster, 1. 31g, 5mmmmol) in anhydrous toluene (10mL) was heated to 80C and treated with a solution of N, N- dimethyl fonnamide di-t-butyl acetal. After 2 h the reaction mixture was cooled to ambient temperature and subjected to flash column chromatography on silica gel (23-400 mesh) using 10% ethyl acetate in hexane as the eluent to afford the title compound (0.7g, 44%). 1H NMR (300 MHz, CDCl3) : 8 7.62 (d, 2H, J= 8.2Hz), 7.01 (d, 2H, J= 8.2Hz), 3. 45 (s, 2H), 1.43 (s, 9H).
44% In toluene; at 80℃; for 2h; 4-Iodo-tert-butyl phenvl acetate (Reagent 10); A solution of 4-iodo phenyl acetic acid (Lancaster, 1. 31g, 5mmmol) in anhydrous toluene (lOmL) was heated to 80C and treated with a solution of N, N- dimethyl formamide di-t-butyl acetal. After 2 h the reaction mixture was cooled to ambient temperature and subjected to flash column chromatography on silica gel (23-400 mesh) using 10% ethyl acetate in hexane as the eluent to afford the title compound (0.7g, 44%). IH NMR (300 MHz, CDCl3) : 8 7.62 (d, 2H, J= 8. 2Hz), 7.01 (d, 2H, J= 8. 2Hz), 3.45 (s, 2H), 1.43 (s, 9H).
  • 3
  • [ 24424-99-5 ]
  • [ 1798-06-7 ]
  • [ 856250-87-8 ]
YieldReaction ConditionsOperation in experiment
5.49 g With dmap; In tert-butyl alcohol; at 20℃; for 3h; To a solution of <strong>[1798-06-7](4-iodophenyl)acetic acid</strong> (5.00 g)in tert-butyl alcohol (40.0 mL), 4-dimethylaminopyridine (0.699 g)and di-tert-butyl dicarbonate (8.33 g)were added and stirred at room temperature for 3 hours. After concentrating the reaction solution under reduced pressure, the residue was purified by silica gel column chromatography (hexane/chloroform)to obtain the title compound (5.48 g)as an oil. 1H-NMR (CDCl3)δ: 1.43 (9H, s), 3.46 (2H, s), 7.02 (2H, d, J = 8.5 Hz), 7.64 (2H, d, J = 8.5 Hz).
 

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