Thionyl Chloride → 5-(Chloromethyl)-1-[4-(pentafluoro-lambda6-sulfanyl)phenyl]-1H-tetrazole
反応式
[F:1][S:2]([F:19])([F:18])([F:17])([F:16])[C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:13]([CH2:14]O)=[N:12][N:11]=[N:10]2)=[CH:5][CH:4]=1.O=S(Cl)[Cl:22]>C1(C)C=CC=CC=1>[Cl:22][CH2:14][C:13]1[N:9]([C:6]2[CH:7]=[CH:8][C:3]([S:2]([F:19])([F:18])([F:17])([F:16])[F:1])=[CH:4][CH:5]=2)[N:10]=[N:11][N:12]=1参加物
4
実験手順
Thionyl chloride (1.72 g, 14.4 mmol) was added to a stirred solution of {1-[4-(pentafluoro-λ6-sulfanyl)phenyl]-1H-tetrazol-5-yl}methanol (Intermediate 44, 3.50 g, 11.6 mmol) in toluene (40 mL), SOCl2 at room temperature. The reaction mixture was stirred for 4 hr at reflux. The reaction mixture was concentrated under vacuum. The residue was diluted with DCM and washed with ice-water, saturated aq NaHCO3 and brine solution, dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the crude compound. This was purified by column chromatography (100-200 mesh silica gel), eluted with 20%-30% EtOAc/pet-ether to give the title compound as a brown gum (3.50 g).