Iodine → 4-[2-[(E)-2-iodovinyl]-phenoxy]butyric acid ethyl ester

HRID 2081311노트

반응식

HRID 2081311 반응식
[CH2:1]([O:3][C:4](=[O:16])[CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1Br)[CH3:2].C([Sn](CC[CH2:43][CH3:44])(CCCC)/C=C/[Sn](CCCC)(CCCC)CCCC)CCC.[I:45]I>C1(C)C=CC=CC=1.C(OCC)C.[Pd].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>[CH2:1]([O:3][C:4](=[O:16])[CH2:5][CH2:6][CH2:7][O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1/[CH:44]=[CH:43]/[I:45])[CH3:2]

참가 물질

7

실험 절차

861 mg of 4-(2-bromophenoxy)-butyric acid ethyl ester and 4.8 g of (E)-1,2-bis-(tri-n-butylstannyl)-ethylene (50%) are dissolved in 11 ml of toluene, mixed with 70 mg of tetrakis-(triphenylphosphine)-palladium and heated with stirring and under argon atmosphere for 1 hour to 120° C. (bath temperature). After cooling to room temperature, the reaction mixture is diluted with 9 ml of diethyl ether and mixed at 0° C. with a solution of 1.53 g of iodine in 7 ml of diethyl ether. The mixture is stirred for 2 hours at 0° C. and allowed to stand overnight in a refrigerator. The batch is concentrated by evaporation and the residue is chromatographed on silica gel with n-hexane/ethyl acetate=95/5. 810 mg of 4-[2-[(E)-2-iodovinyl]-phenoxy]-butyric acid ethyl ester is obtained as an oily crude product, which is further reacted without further purification.

후처리

  1. temperatureheated
  2. stirringThe mixture is stirred for 2 hours at 0° C.
  3. concentrationThe batch is concentrated by evaporation
  4. customthe residue is chromatographed on silica gel with n-hexane/ethyl acetate=95/5

출처 및 근거

ORD 기록
ord-ad9f42c333444e65a5b68150132b5bb3
출처 데이터셋
uspto-grants-1993_02
특허 번호
US05183925

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