1: 1.) Mg; MeI / diethyl ether / 1.) 3 h, reflux; 2.) 1 h, reflux 2: hydrogen, conc. H2SO4 / 10percent Pd-C / ethyl acetate / 4 h / 2942.03 Torr / Ambient temperature 3: ethanethiol, NaH / dimethylformamide / 3 h / Heating View Scheme

1: hydrogen, conc. H2SO4 / 10percent Pd-C / ethyl acetate / 4 h / 2942.03 Torr / Ambient temperature 2: ethanethiol, NaH / dimethylformamide / 3 h / Heating View Scheme

1: 89 percent / (COCl)2 / benzene / 2 h, room t., 1 h, reflux 2: 70 percent / NaOAc, H2 / 10percent Pd-C / 2427.2 Torr / 1h, then 60 degC, overnight 3: 1.) Mg; MeI / diethyl ether / 1.) 3 h, reflux; 2.) 1 h, reflux 4: hydrogen, conc. H2SO4 / 10percent Pd-C / ethyl acetate / 4 h / 2942.03 Torr / Ambient temperature 5: ethanethiol, NaH / dimethylformamide / 3 h / Heating View Scheme

1: 70 percent / NaOAc, H2 / 10percent Pd-C / 2427.2 Torr / 1h, then 60 degC, overnight 2: 1.) Mg; MeI / diethyl ether / 1.) 3 h, reflux; 2.) 1 h, reflux 3: hydrogen, conc. H2SO4 / 10percent Pd-C / ethyl acetate / 4 h / 2942.03 Torr / Ambient temperature 4: ethanethiol, NaH / dimethylformamide / 3 h / Heating View Scheme

iodine 0.5 h; Heating;

sodium hydride; ethanethiol in N,N-dimethyl-formamide 3 h; Heating;

0.25 h; 90-100 deg C, 15 min, then sublimed under vacuum 15 mmHg at 100-120 deg C;

暂无反应条件数据

trimethylsilyl iodide; N,N,N',N,-tetramethylethylenediamine; sec.-butyllithium 1) Et2O, 2) CH3CN, heating; Yield given. Multistep reaction;

methanol; potassium hydroxide T=130 - 135°C;