反应 #4123114
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8c8b729f7c2f46ae967ab7cbc492e7d8暂无可渲染的结构数据
C(C(F)(F)F)NC(=S)N产品信息
2,2,2-trifluoroethylthiourea(CAS 84545-31-3)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8c8b729f7c2f46ae967ab7cbc492e7d8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2,2,2-trifluoroethylthiourea (8.0 g.) and methyl iodide (3.5 g.) in EtOH (40 ml.) was heated under reflux for 70 minutes, then evaporated to dryness in vacuo. The residue was triturated with ether to give 2,2,2-trifluoroethyl-S-methylisothiourea hydroiodide, m.p. 154°-156° (90%). under reflux for 70 minutes evaporated to dryness in vacuo The residue was triturated with ether
来源 ID: ord-4960a60ca38242b3bae6f6cece2e2d00反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2,2,2-trifluoroethylthiourea (8.0 g.) and methyl iodide (3.5 g.) in EtOH (40 ml.) was heated under reflux for 70 minutes, then evaporated to dryness in vacuo. The residue was triturated with ether to give 2,2,2-trifluoroethyl-S-methylisothiourea hydroiodide, m.p. 154°-156° (90%). under reflux for 70 minutes evaporated to dryness in vacuo The residue was triturated with ether
来源 ID: ord-eb664b0dcd9f44d985ecb0985c5b3da2反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2,2,2-trifluoroethylthiourea (8.0 g.) and methyl iodide (3.5 g.) in EtOH (40 ml.) was heated under reflux for 70 minutes, then evaporated to dryness in vacuo. The residue was triturated with ether to give 2,2,2-trifluoroethyl-S-methylisothiourea hydroiodide, m.p. 154°-156° (90%). under reflux for 70 minutes evaporated to dryness in vacuo The residue was triturated with ether
来源 ID: ord-eb664b0dcd9f44d985ecb0985c5b3da2反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8c8b729f7c2f46ae967ab7cbc492e7d8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Slurry 4-cyanophenacyl bromide (1.4 g, 6.3 mmol), 2,2,2-trifluoroethyl-thiourea (1.0 g, 6.3 mmol) and sodium bicarbonate (529 mg, 6.3 mmol) in absolute ethanol (30 mL). Stir the mixture at reflux for 1 h under a nitrogen atmosphere. Cool to room temperature and concentrate in vacuo. Partition the residue between DCM (100 mL) and water (20 mL). Dry the organic layer over Na2SO4 and concentrate in vacuo to obtain the desired intermediate (1.7 g, 95%). MS (ES+) m/z: 284 (M+H)+. at reflux for 1 h under a nitrogen atmosphere concentrate in vacuo Partition the residue between DCM (100 mL) and water (20 mL) Dry the organic layer over Na2SO4 concentrate in vacuo
来源 ID: ord-d4a371b13503439f922b45fee5d47658反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Slurry 1-benzoyl-3-(2,2,2-trifluoroethyl)-thiourea (5.5 g, 21.2 mmol) and potassium carbonate (11.7 g, 84.7 mmol) in methanol (180 mL) and water (40 mL). Stir the mixture at room temperature for 16 h. Concentrate the solution in vacuo to a paste. Triturate with hot water (20 mL, 60° C.), filter off the solids, wash with water (20 mL, 25° C.) and hexane (excess). Collect the solids, slurry in EtOAc and concentrate in vacuo twice to remove residual water. Dry the material in a vacuum oven at 45° C. for 16 h to obtain the desired intermediate as an off-white solid (2.2 g, 66%). MS (ES+) m/z: 159.1 (M+H)+. Concentrate the solution in vacuo to a paste Triturate with hot water (20 mL, 60° C.) filter off the solids wash with water (20 mL, 25° C.) and hexane (excess) Collect the solids, slurry in EtOAc concentrate in vacuo twice to remove residual water Dry the material in a vacuum oven at 45° C. for 16 h
来源 ID: ord-da0721c021574b16ad5c902124d32dfd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2,2,2-trifluoroethylthiourea (8.0 g.) and methyl iodide (3.5 g.) in EtOH (40 ml.) was heated under reflux for 70 minutes, then evaporated to dryness in vacuo. The residue was triturated with ether to give 2,2,2-trifluoroethyl-S-methylisothiourea hydroiodide, m.p. 154°-156° (90%). under reflux for 70 minutes evaporated to dryness in vacuo The residue was triturated with ether
来源 ID: ord-4960a60ca38242b3bae6f6cece2e2d00反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 2,2,2-trifluoroethylthiourea (8.0 g.) and methyl iodide (3.5 g.) in EtOH (40 ml.) was heated under reflux for 70 minutes, then evaporated to dryness in vacuo. The residue was triturated with ether to give 2,2,2-trifluoroethyl-S-methylisothiourea hydroiodide, m.p. 154°-156° (90%). under reflux for 70 minutes evaporated to dryness in vacuo The residue was triturated with ether
来源 ID: ord-eb664b0dcd9f44d985ecb0985c5b3da2PubChem References
以下资料来自该化合物的公开数据库参考记录。
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