反应 #4158005
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-730eb7d4b994476b80b2b8618068e7c4暂无可渲染的结构数据
C1C2=C(C=C(C=C2)Cl)NC1=O产品信息
6-氯氧化吲哚(CAS 56341-37-8)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-730eb7d4b994476b80b2b8618068e7c4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-95670aefdabb4830918d38306bc14f72反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-1c1d1f0005af478eb5b879da5740fcd3反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5ed8a1cbff4a42be8dc5df71c60477cf反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ba4cafacff5a48bdb0b936fe8df8dad9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-643c436d6dba4ad7b9794b58f65fccca反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f55d9be8dd8a4c2097d1e850bdd56b73反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-876b8a449d5c42239fdb7ff34a4f4eb5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-647e1091419c44b59cd0969e4bb4a68f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Under argon atmosphere, 3,5-bis(trifluoromethyl)isocyanate (255 mg, 1.0 mmol) was dissolved in tetrahydrofuran (5 mL). A solution of 6-chloro-oxindole (184 mg, 1.1 mmol) in tetrahydrofuran (5 ml) and triethylamine (0.3 mL) were added, and the mixture was stirred at room temperature for 4 hours. The reaction mixture was poured into diluted hydrochloric acid and extracted with ethyl acetate. After the organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, the residue obtained by evaporation under reduced pressure was purified by chromatography on silica gel (n-hexane:ethyl acetate=4:1) to give the title compound (172.2 mg, 40.7%) as a pink solid. extracted with ethyl acetate After the organic layer was washed with water and brine dried over anhydrous magnesium sulfate the residue obtained by evaporation under reduced pressure was purified by chromatography on silica gel (n-hexane:ethyl acetate=4:1)
来源 ID: ord-4439cdd7b9dd4d138986a56fb2e2e9af反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the mixture of 6-chloro-2-oxindole (4.4 g, 26 mmol) (Crescent) and 3-chloro-5-fluorobenzaldehyde (4.2 g, 26 mmol) (Aldrich) in methanol (200 mL) was added piperidine (2.3 g, 26 mmol) (Aldrich) dropwise. The mixture was then heated at 80° C. for 2 h. After cooled to 4° C., the mixture was filtered and resulting precipitate was collected, dried to give E/Z-6-chloro-3-(3-chloro-5-fluoro-benzylidene)-1,3-dihydro-indol-2-one as a yellow solid (Yield 7.5 g, 92%). After cooled to 4° C. the mixture was filtered resulting precipitate was collected dried
来源 ID: ord-351820dab05141fe95a65030707b7a6e反应条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To the mixture of 6-chloro-2-oxindole (5.3 g, 32 mmol) (Crescent) and 3-chloro-4-fluorobenzaldehyde (5 g, 32 mmol) (Aldrich) in methanol (200 mL) was added piperidine (2.7 g, 32 mmol) (Aldrich) dropwise. The mixture was then heated at 50° C. for 3 h. After cooled to 4° C., the mixture was filtered and resulting precipitate was collected, dried to give E/Z-6-chloro-3-(3-chloro-4-fluoro-benzylidene)-1,3-dihydro-indol-2-one as a yellow solid (Yield 8 g, 82%). After cooled to 4° C. the mixture was filtered resulting precipitate was collected dried
来源 ID: ord-95ea907173fb4b349def638a76895dbfPubChem References
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