反应 #4149378
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-532b552e685543b6a1901ca63486044a暂无可渲染的结构数据
CCOC(=O)C1=C(C=C(C=C1)F)F产品信息
2,4-二氟苯甲酸乙酯(CAS 108928-00-3)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 2737170
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-532b552e685543b6a1901ca63486044a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-86c371f6f5c8423a8e63903b1030ade8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9dd775632d734af4821d4eff7736aa4a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8dc75e759e6646e4a5c0d338ef77a5ae反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-532b552e685543b6a1901ca63486044a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-86c371f6f5c8423a8e63903b1030ade8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-86c371f6f5c8423a8e63903b1030ade8反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Ethyl 2,4-difluorobenzoate (1.14 g), K3PO4 (1.30 g) and 5-hydroxyindazole (0.90 g) were stirred at 110° C. in diglyme (12 mL) for 24 hours. The reaction was cooled and poured into ether. The solution was washed three times with 1M NaOH solution, and brine, and dried. The solution was then concentrated, and the crude product was chromatographed on silica gel with 20% ethyl acetate/hexanes. The reaction was cooled The solution was washed three times with 1M NaOH solution, and brine dried The solution was then concentrated the crude product was chromatographed on silica gel with 20% ethyl acetate/hexanes
来源 ID: ord-9381d47dd24e46eeb134ed4fe7eaa600反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Ethyl 2,4-difluorobenzoate (1.14 g), K3PO4 (1.30 g) and 5-hydroxyindazole (0.90 g) were stirred at 110° C. in diglyme (12 mL) for 24 hours. The reaction was cooled and poured into ether. The solution was washed three times with 1M NaOH solution, and brine, and dried. The solution was then concentrated, and the crude product was chromatographed on silica gel with 20% ethyl acetate/hexanes. The reaction was cooled The solution was washed three times with 1M NaOH solution, and brine dried The solution was then concentrated the crude product was chromatographed on silica gel with 20% ethyl acetate/hexanes
来源 ID: ord-9381d47dd24e46eeb134ed4fe7eaa600反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared by substituting 3-amino-2-methylphenol for 2-methyl-5-indolol and methyl 2,4-difluorobenzoate for ethyl 2,4-difluorobenzoate in EXAMPLE 3A.
来源 ID: ord-2b1f4f18a7ac4c8d901e6197b96a6bee反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared by substituting 3-amino-2-methylphenol for 2-methyl-5-indolol and methyl 2,4-difluorobenzoate for ethyl 2,4-difluorobenzoate in EXAMPLE 3A.
来源 ID: ord-2b1f4f18a7ac4c8d901e6197b96a6bee反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared by substituting methyl 2,4-difluorobenzoate for ethyl 2,4-difluorobenzoate and 5-hydroxy-3,4-dihydro-2H-isoquinolin-1-one for 2-methyl-5-indolol in EXAMPLE 3A, except here the heating was at 130° C. was at 130° C.
来源 ID: ord-0ca5d2474e194cba960d6ac4b95f5fe5PubChem 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 85070-58-2
CAS 394-35-4
CAS 106614-28-2
CAS 1415124-73-0
CAS 351354-41-1
CAS 2967-93-3
CAS 773134-91-1
CAS 362601-90-9
CAS 496841-90-8
CAS 351354-50-2
CAS 1162674-66-9
CAS 79538-30-0
