反応 #3860514
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-ae6199f9700b41a495bb6a085c783489表示可能な構造データがありません
C1=CC(=C(C=C1Br)N)C(F)(F)F製品情報
5-bromo-2-(trifluoromethyl)aniline (CAS 703-91-3) 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 25067357
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
5 反応 · 5 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ae6199f9700b41a495bb6a085c783489反応条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 5-bromo-2-(trifluoromethyl)aniline (3.0 g, 12.6 mmol), glycerol (4.64 g, 50.0 mmol), and ferrous sulfate (0.56 g, 2.0 mmol) was added conc. sulfuric acid (2.2 mL) dropwise. The reaction mixture was heated at 120° C. for 4 hr. After cooled to RT, the reaction was diluted with ethyl acetate (150 mL), and 2N aq. NaOH was introduced to adjust pH about 13. The organic layer was separated and washed with brine and dried over Na2SO4 and evaporated to give the crude product, which was purified with flash column chromatography to give 5-bromo-8-(trifluoromethyl)quinoline (1.2 g, 48%). After cooled to RT was introduced The organic layer was separated washed with brine dried over Na2SO4 evaporated to give the crude product, which was purified with flash column chromatography
ソース ID: ord-3915d672e1e743f59b2d87d94aa2f5e0反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of 4-bromo-2-nitro-1-(trifluoromethyl)benzene (4.0 g, 14.9 mmol) in ethanol (230 mL), THF (85 mL), and water (40 mL) was added ammonium chloride (1.0 g, 18.8 mmol) and ferrous powder (5.06 g, 90 mmol). The resulting mixture was heated at 80° C. for 1 hr and the progress of the reaction was monitored by TLC. Upon complete consumption of staring material, the reaction mixture was filtered off while it was hot. The filtrate was evaporated under vacuum and the crude residue was diluted with ethyl acetate (100 mL) and washed with water (3×50 mL). The combined organic layer was washed with brine, dried over Na2SO4 and evaporated under vacuum to afford 5-bromo-2-(trifluoromethyl)aniline as a solid (3.2 g, 90%). Upon complete consumption of staring material the reaction mixture was filtered off while it The filtrate was evaporated under vacuum the crude residue was diluted with ethyl acetate (100 mL) washed with water (3×50 mL) The combined organic layer was washed with brine dried over Na2SO4 evaporated under vacuum
ソース ID: ord-6a40f54a3bd4439c89af9fb70f7e46bb反応条件: temp:120.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a mixture of 5-bromo-2-(trifluoromethyl)aniline (3.0 g, 12.6 mmol), glycerol (4.64 g, 50.0 mmol), and ferrous sulfate (0.56 g, 2.0 mmol) was added conc. sulfuric acid (2.2 mL) dropwise. The reaction mixture was heated at 120° C. for 4 hr. After cooled to RT, the reaction was diluted with ethyl acetate (150 mL), and 2N aq. NaOH was introduced to adjust pH about 13. The organic layer was separated and washed with brine and dried over Na2SO4 and evaporated to give the crude product, which was purified with flash column chromatography to give 5-bromo-8-(trifluoromethyl)quinoline (1.2 g, 48%). After cooled to RT was introduced The organic layer was separated washed with brine dried over Na2SO4 evaporated to give the crude product, which was purified with flash column chromatography
ソース ID: ord-dd5cfdef257a480bbeda532188eb3058反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: To a suspension of 4-bromo-2-nitro-1-(trifluoromethyl)benzene (4.0 g, 14.9 mmol) in ethanol (230 mL), THF (85 mL), and water (40 mL) was added ammonium chloride (1.0 g, 18.8 mmol) and ferrous powder (5.06 g, 90 mmol). The resulting mixture was heated at 80° C. for 1 hr and the progress of the reaction was monitored by TLC. Upon complete consumption of staring material, the reaction mixture was filtered off while it was hot. The filtrate was evaporated under vacuum and the crude residue was diluted with ethyl acetate (100 mL) and washed with water (3×50 mL). The combined organic layer was washed with brine, dried over Na2SO4 and evaporated under vacuum to afford 5-bromo-2-(trifluoromethyl)aniline as a solid (3.2 g, 90%). Upon complete consumption of staring material the reaction mixture was filtered off while it The filtrate was evaporated under vacuum the crude residue was diluted with ethyl acetate (100 mL) washed with water (3×50 mL) The combined organic layer was washed with brine dried over Na2SO4 evaporated under vacuum
ソース ID: ord-d885e98df8414def9d1a4e7ebedcdc74PubChem 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。
関連製品
12 related records
CAS 402-43-7
CAS 244246-71-7
CAS 455-14-1
CAS 58458-13-2
CAS 67169-22-6
CAS 25449-96-1
CAS 54962-75-3
CAS 54396-44-0
CAS 328-93-8
CAS 1219795-48-8
CAS 57946-63-1
CAS 88301-98-8
見積依頼
仕様、数量、納入先、用途をご連絡ください。供給可否を確認します。
