Methyl Acrylate → (E)-3-(2-methyl-benzothiazol-6-yl)-acrylic acid methyl ester

HRID 1469649

Reaktionsgleichung

Reaktionsgleichung von HRID 1469649
I[C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([CH3:9])[S:8][C:4]=2[CH:3]=1.[C:12]([O:16][CH3:17])(=[O:15])[CH:13]=[CH2:14].C(N(CC)CC)C>C(O[Pd]OC(=O)C)(=O)C>[CH3:17][O:16][C:12](=[O:15])/[CH:13]=[CH:14]/[C:2]1[CH:11]=[CH:10][C:5]2[N:6]=[C:7]([CH3:9])[S:8][C:4]=2[CH:3]=1

Komponenten

5

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of 6-iodo-2-methylbenzo[d]thiazole (275 mg, 1 mmol), methyl acrylate (103 mg, 1.2 mmol), diacetoxypalladium (22 mg, 0.1 mmol) and triethylamine (304 mg, 3 mmol) MeCN (8 mL) is heated in a microwave apparatus at 100° C. for 10 min. The solvent is removed under reduce pressure and the residue is purified by flash chromatography (heptane:EtOAc, 2:1) to give (E)-3-(2-methyl-benzothiazol-6-yl)-acrylic acid methyl ester. MS 234.3 (M+1).

Aufarbeitung

  1. customThe solvent is removed
  2. customthe residue is purified by flash chromatography (heptane:EtOAc, 2:1)

Quellen und Nachweise

ORD-Eintrag
ord-c7874f8223fe480ba751f892847c0abd
Quelldatensatz
uspto-grants-2015_04
Patentnummer
US09006249B2

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