反应 #2207394
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openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US06818663B2
反应条件: temp:-15.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a cooled (−15° C.) solution of 1,1-thiocarbonyidiimidazole (756 mg, 4.115 mmol) (Aldrich) in N,N-dimethylformamide (11 mL) was added dropwise a solution of [3-(4-aminophenoxy)propyl]carbamic acid tert-butyl ester (1.02 g, 3.84 mmol) (from Step B above) in N,N-dimethylformamide (11 mL) over 25 minute. After the addition was complete, the mixture was stirred at −15° C. for 20 minute and then at room temperature for 1 h. Ice-water was added and the mixture was extracted with ether. The ether layer was dried (MgSO4), filtered, and evaporated. The residue was purified on silica gel with 85:15 hexane/ethyl acetate to give [3-(4-isothiocyanatophenoxy)propyl]-carbamic acid tert-butyl ester (1.07 g, 91% yield). HRMS, observed: 308.1197; Calcd for M+:308.1195. After the addition at room temperature for 1 h the mixture was extracted with ether The ether layer was dried (MgSO4) filtered evaporated The residue was purified on silica gel with 85:15 hexane/ethyl acetate
来源 ID: ord-6afbc6a0bc0749cc81ba42a98d3b7ac2