反応 #4108358
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-08d992371bdc447caeb694aa36674df5表示可能な構造データがありません
C1=CC=C(C=C1)COC2=C(C=C(C=C2Cl)N)Cl製品情報
3,5-dichloro-4-phenylmethoxyaniline (CAS 848133-04-0) 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 18543171
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
7 反応 · 7 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-08d992371bdc447caeb694aa36674df5反応条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Cesium carbonate (5.98 g, 19 mmol) was added to a stirring solution of 4-(benzyloxy)-3,5-dichloroaniline (5.27 g [crude from previous step], 19 mmol) in toluene. Rac-BINAP (0.6 g, 7.5 mol %) and methyl 2-bromobenzoate (1.84 ml 13 mmol,) were added. Palladium(II) acetate (0.147 g, 5 mol %) was added and the mixture heated to 100° C. After 12 h the mixture was cooled to room temperature, diluted with ethyl acetate (100 mL), washed with pH 7 buffer solution (50 mL) and extracted with ethyl acetate (100 mL). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo to afford a residue that was purified by column chromatography (3:1, petroleum ether/dichloromethane) to afford methyl 2-(4-(benzyloxy)-3,5-dichlorophenylamino)benzoate as a white solid (94% yield). After 12 h the mixture was cooled to room temperature washed with pH 7 buffer solution (50 mL) extracted with ethyl acetate (100 mL) The combined organic layers were dried (MgSO4) filtered concentrated in vacuo to afford a residue that was purified by column chromatography (3:1, petroleum ether/dichloromethane)
ソース ID: ord-980be7ca4be946f0bca7a4c36ce8724a反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Tin(II) chloride (22 g, 98 mmol) was added to a stirring solution of 2-(benzyloxy)-1,3-dichloro-5-nitrobenzene (5.8 g, 19 mmol) in ethanol (80 mL), and the resulting suspension was heated to 70° C. After 1 h the mixture was cooled to room temperature and diluted with ethyl acetate (200 mL). The mixture was poured into brine (100 mL) and the resulting emulsion stirred with sodium potassium tartrate solution (200 mL). The mixture was extracted with ethyl acetate and the combined organic layers dried (MgSO4), filtered and concentrated in vacuo to afford 4-(benzyloxy)-3,5-dichloroaniline that was used directly in the next step without purification. After 1 h the mixture was cooled to room temperature The mixture was extracted with ethyl acetate the combined organic layers dried (MgSO4) filtered concentrated in vacuo
ソース ID: ord-3cc40db0e4aa49bfb82c4e603f980a5f反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Tin(II) chloride (22 g, 98 mmol) was added to a stirring solution of 2-(benzyloxy)-1,3-dichloro-5-nitrobenzene (5.8 g, 19 mmol) in ethanol (80 mL), and the resulting suspension was heated to 70° C. After 1 h the mixture was cooled to room temperature and diluted with ethyl acetate (200 mL). The mixture was poured into brine (100 mL) and the resulting emulsion stirred with sodium potassium tartrate solution (200 mL). The mixture was extracted with ethyl acetate and the combined organic layers dried (MgSO4), filtered and concentrated in vacuo to afford 4-(benzyloxy)-3,5-dichloroaniline that was used directly in the next step without purification. After 1 h the mixture was cooled to room temperature The mixture was extracted with ethyl acetate the combined organic layers dried (MgSO4) filtered concentrated in vacuo
ソース ID: ord-3cc40db0e4aa49bfb82c4e603f980a5f反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-08d992371bdc447caeb694aa36674df5反応条件: temp:100.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Cesium carbonate (5.98 g, 19 mmol) was added to a stirring solution of 4-(benzyloxy)-3,5-dichloroaniline (5.27 g [crude from previous step], 19 mmol) in toluene. Rac-BINAP (0.6 g, 7.5 mol %) and methyl 2-bromobenzoate (1.84 ml 13 mmol,) were added. Palladium(II) acetate (0.147 g, 5 mol %) was added and the mixture heated to 100° C. After 12 h the mixture was cooled to room temperature, diluted with ethyl acetate (100 mL), washed with pH 7 buffer solution (50 mL) and extracted with ethyl acetate (100 mL). The combined organic layers were dried (MgSO4), filtered and concentrated in vacuo to afford a residue that was purified by column chromatography (3:1, petroleum ether/dichloromethane) to afford methyl 2-(4-(benzyloxy)-3,5-dichlorophenylamino)benzoate as a white solid (94% yield). After 12 h the mixture was cooled to room temperature washed with pH 7 buffer solution (50 mL) extracted with ethyl acetate (100 mL) The combined organic layers were dried (MgSO4) filtered concentrated in vacuo to afford a residue that was purified by column chromatography (3:1, petroleum ether/dichloromethane)
ソース ID: ord-980be7ca4be946f0bca7a4c36ce8724a反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Tin(II) chloride (22 g, 98 mmol) was added to a stirring solution of 2-(benzyloxy)-1,3-dichloro-5-nitrobenzene (5.8 g, 19 mmol) in ethanol (80 mL), and the resulting suspension was heated to 70° C. After 1 h the mixture was cooled to room temperature and diluted with ethyl acetate (200 mL). The mixture was poured into brine (100 mL) and the resulting emulsion stirred with sodium potassium tartrate solution (200 mL). The mixture was extracted with ethyl acetate and the combined organic layers dried (MgSO4), filtered and concentrated in vacuo to afford 4-(benzyloxy)-3,5-dichloroaniline that was used directly in the next step without purification. After 1 h the mixture was cooled to room temperature The mixture was extracted with ethyl acetate the combined organic layers dried (MgSO4) filtered concentrated in vacuo
ソース ID: ord-3cc40db0e4aa49bfb82c4e603f980a5fPubChem 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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