Iodine → Ethyl 3-(2-iodo-5-methoxyphenyl)propionate

HRID 2044185Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2044185
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:9][CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])[CH:6]=[CH:7][CH:8]=1.[I:16]I.C([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)CCC>C(#N)C>[I:16][C:6]1[CH:7]=[CH:8][C:3]([O:2][CH3:1])=[CH:4][C:5]=1[CH2:9][CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12]

Komponenten

5

Edukt 3

HCID 807IodineHCID 159629ButyltriphenylphosphoniumHCID 584318Ethyl 3-(3-methoxyphenyl)propanoate

Produkt 1

HCID 11110409Ethyl 3-(2-iodo-5-methoxyphenyl)propionateAusbeute 76 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

To a solution of ester 25 (1.618 g, 7.77 mmol) in acetonitrile (100 mL), iodine (1.972 g, 7.77 mmol) and n-butyltriphenylphosphonium peroxodisulfate (6.455 g, 7.77 mmol) were added and refluxed for 45 min. The reaction mixture was cooled to room temperature and the excess of iodine was removed by dropwise addition of 1M Na2S2O3 solution. The colourless solution was transferred to a separatory funnel and the organic layer was separated and dried over Na2SO4. Evaporation of the solvent followed by means of column chromatography on silica gel (hexane/isopropylether 10:1) gave 1.982 mg of iodinated ester 26 as a yellowish oil. Yield 76%. 1H NMR (300 MHz, CDCl3) δ ppm: 7.65 (d, J=8.7 Hz, 1H), 6.82 (d, J=3.0 Hz, 1H), 6.51 (dd, J1=8.7 Hz, J2=3.0 Hz, 1H), 4.14 (q, J=7.1 Hz, 2H), 3.76 (s, 3H), 3.00 (t, J=7.9 Hz, 2H), 2.60 (t, J=7.9 Hz, 2H), 1.25 (t, J=7.1 Hz, 3H); 13C NMR (75 MHz, CDCl3) δ ppm: 172.4, 160.0, 144.0, 139.9, 115.5, 114.1, 88.6, 60.5, 55.3, 35.9, 34.4, 14.2; HRMS (EI) m/z: calcd for C12H15|O3: 334.0065. found: 334.0082.

Aufarbeitung

  1. temperaturerefluxed for 45 min
  2. customthe excess of iodine was removed by dropwise addition of 1M Na2S2O3 solution
  3. customThe colourless solution was transferred to a separatory funnel
  4. customthe organic layer was separated
  5. dry with materialdried over Na2SO4
  6. customEvaporation of the solvent

Quellen und Nachweise

ORD-Eintrag
ord-1259d980fdb747048d72a771824451db
Quelldatensatz
uspto-grants-2013_11
Patentnummer
US08586776B2

Notizen zur Reaktion

Wird geladen…