反应 #4151022
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-4e8dca35b57d4dd99659253cd05f18ff暂无可渲染的结构数据
C1=CC(=CC=C1C#N)S产品信息
4-巯基苯甲腈(CAS 36801-01-1)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 585058
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4e8dca35b57d4dd99659253cd05f18ff反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ede0d5cdc8844e5a888d57965d81dd36反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1d0c7a0b3e44453191db16351873683c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4567844ed3744c1683fa86b76a6c4813反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-232a1f6dd4b24aafbe7c5ef51c1fd012反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bb3f107647d1480bb19922382b935072反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-cyanothiophenol (20.8 g, 154 mmol), 1,3-dibromopropane (155 g, 0.77 mol) and K2CO3 (21.3 g, 154 mmol) in MeCN (300 mL) was refluxed overnight. Filtration and evaporation of the solvent gave a brown oil that crystallised when treated with EtOH. The crystals were isolated by filtration to give the sub-title compound (24.5 g, 62%). was refluxed overnight Filtration and evaporation of the solvent gave a brown oil that crystallised when treated with EtOH The crystals were isolated by filtration
来源 ID: ord-e210cc88553e41ccbd065dfcac3ebcaa反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-cyanothiophenol (20.8 g, 154 mmol), 1,3-dibromopropane (155 g, 0.77 mol) and K2CO3 (21.3 g, 154 mmol) in MeCN (300 mL) was refluxed overnight. Filtration and evaporation of the solvent gave a brown oil that crystallised when treated with EtOH. The crystals were isolated by filtration to give the sub-title compound (24.5 g, 62%). was refluxed overnight Filtration and evaporation of the solvent gave a brown oil that crystallised when treated with EtOH The crystals were isolated by filtration
来源 ID: ord-b475c840d01848b8a235b976bc7674b3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of potassium hydroxide (7.5 g) in a mixture of ethanol (220 ml) and water (55 ml) was added at ambient temperature under nitrogen to a stirred solution of 4-mercaptobenzonitrile (18.0 g; prepared according to the method of S. Krishnamurthy and D. Aimino, J. Org. Chem., 1989, 54, 4458) in a mixture of ethanol (195 ml) and water (12 ml), then the mixture was stirred at ambient temperature for 4.5 hours. A solution of 1-chloro-4-phenoxybut-2-yne (24.1 g; prepared in a similar manner to that described in Example 5) in a mixture of ethanol (195 ml) and water (12 ml) was added dropwise over 1.5 hours, then the mixture was stirred at ambient temperature for 17 hours. The mixture was concentrated in vacuo to remove the ethanol, then the product was diluted with water (150 ml) and extracted into ethyl acetate (2×250 ml). The combined extracts were washed with water (100 ml) and saturated brine (100 ml), dried (MgSO4), and the solvent removed in vacuo to leave 4-(4-phenoxybut-2-ynylthio)benzonitrile as an off-white solid (37.7 g). prepared prepared in a similar manner to that was added dropwise over 1.5 hours the mixture was stirred at ambient temperature for 17 hours The mixture was concentrated in vacuo to remove the ethanol the product was diluted with water (150 ml) extracted into ethyl acetate (2×250 ml) The combined extracts were washed with water (100 ml) and saturated brine (100 ml) dried (MgSO4) the solvent removed in vacuo
来源 ID: ord-a805daa329c6473aafeb2d7e69fddb35反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-4e8dca35b57d4dd99659253cd05f18ff反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ede0d5cdc8844e5a888d57965d81dd36反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ede0d5cdc8844e5a888d57965d81dd36PubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 34761-11-0
CAS 39718-07-5
CAS 100-47-0
CAS 1374518-05-4
CAS 104-85-8
CAS 22445-42-7
CAS 623-26-7
CAS 174658-22-1
CAS 64409-12-7
CAS 868525-07-9
CAS 77474-63-6
CAS 54435-88-0
