反応 #4149378
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-532b552e685543b6a1901ca63486044a表示可能な構造データがありません
CCOC(=O)C1=C(C=C(C=C1)F)F製品情報
ethyl 2,4-difluorobenzoate (CAS 108928-00-3) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 2737170
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-532b552e685543b6a1901ca63486044a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-86c371f6f5c8423a8e63903b1030ade8反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9dd775632d734af4821d4eff7736aa4a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-8dc75e759e6646e4a5c0d338ef77a5ae反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-532b552e685543b6a1901ca63486044a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-86c371f6f5c8423a8e63903b1030ade8反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-86c371f6f5c8423a8e63903b1030ade8反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-9381d47dd24e46eeb134ed4fe7eaa600反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-9381d47dd24e46eeb134ed4fe7eaa600反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-2b1f4f18a7ac4c8d901e6197b96a6bee反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-2b1f4f18a7ac4c8d901e6197b96a6bee反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-0ca5d2474e194cba960d6ac4b95f5fe5PubChem References
化合物の公開データベース記録に掲載された情報源です。
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