반응 #635151

ord-f8d9181bb2b042b99841975848af3728

반응 방정식

CC(C)n1cc(-c2ccc(F)cc2)c2ccccc21
3-(4-fluorophenyl)-1-isopropyl-1H-indole
COC(=O)CC(OC)OC
methyl 3,3-dimethoxypropionate
CC(=O)O
acetic acid
CC(=O)O
acetic acid
O=P(Cl)(Cl)Cl
phosphorus oxychloride
COC(=O)/C=C/c1c(-c2ccc(F)cc2)c2ccccc2n1C(C)C
methyl trans-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylate
수율 93.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타a reaction
  2. 2
    workup.ADDITIONwas added dropwise into the reaction liquid
  3. 3
    여과the precipitated crystals were filtrated
  4. 4
    세척The crystals were washed with 20 vol % aqueous methanol
  5. 5
    기타dried

실험 절차

1.01 g of 3-(4-fluorophenyl)-1-isopropyl-1H-indole, 0.92 g of methyl 3,3-dimethoxypropionate, 0.72 mL of 90 wt % aqueous acetic acid (containing 4 mmol of water) and 6 mL of glacial acetic acid were mixed, then, 0.33 g of phosphorus oxychloride was added dropwise into the mixture at an inner temperature of 25° C., the added mixture was stirred for 9 hours at the same temperature to cause a reaction. After completion of the reaction, 16 mL of water was added dropwise into the reaction liquid, and the precipitated crystals were filtrated. The crystals were washed with 20 vol % aqueous methanol, then, dried to obtain 1.25 g of methyl trans-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylate (yellow solid). Yield: 93%.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07939674B2uspto-grants-2011_05