反応 #4158005
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-730eb7d4b994476b80b2b8618068e7c4表示可能な構造データがありません
C1C2=C(C=C(C=C2)Cl)NC1=O製品情報
6-chloro-1,3-dihydroindol-2-one (CAS 56341-37-8) 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 736344
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-730eb7d4b994476b80b2b8618068e7c4反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-95670aefdabb4830918d38306bc14f72反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1c1d1f0005af478eb5b879da5740fcd3反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5ed8a1cbff4a42be8dc5df71c60477cf反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ba4cafacff5a48bdb0b936fe8df8dad9反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-643c436d6dba4ad7b9794b58f65fccca反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f55d9be8dd8a4c2097d1e850bdd56b73反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-876b8a449d5c42239fdb7ff34a4f4eb5反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-647e1091419c44b59cd0969e4bb4a68f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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)
ソース ID: ord-4439cdd7b9dd4d138986a56fb2e2e9af反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-351820dab05141fe95a65030707b7a6e反応条件: temp:50.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-95ea907173fb4b349def638a76895dbfPubChem 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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