反応 #4014776
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-06db46463df34a549caf9abc3aa1e02f表示可能な構造データがありません
B(C1=CC=CC=C1C(=O)OC(C)C)(O)O製品情報
2-(Isopropoxycarbonyl)phenylboronic acid (CAS 339538-60-2) 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 53435142
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
9 反応 · 9 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-06db46463df34a549caf9abc3aa1e02f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield. the reaction vessel purged 8 ml of a 10% sodium carbonate solution was added the reaction mixture was heated at reflux for 1.5 h The resulting mixture was extracted with ethyl acetate the combined organic layers dried (magnesium sulfate) filtered concentrated under vacuum Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes
ソース ID: ord-8bb323db14634dfba0d4059e3722cebe反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield. the reaction vessel purged 8 ml of a 10% sodium carbonate solution was added the reaction mixture was heated at reflux for 1.5 h The resulting mixture was extracted with ethyl acetate the combined organic layers dried (magnesium sulfate) filtered concentrated under vacuum Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes
ソース ID: ord-8bb323db14634dfba0d4059e3722cebe反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield. the reaction vessel purged 8 ml of a 10% sodium carbonate solution was added the reaction mixture was heated at reflux for 1.5 h The resulting mixture was extracted with ethyl acetate the combined organic layers dried (magnesium sulfate) filtered concentrated under vacuum Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes
ソース ID: ord-3da357480ed243f08b79952da60fad6e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-06db46463df34a549caf9abc3aa1e02f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield. the reaction vessel purged 8 ml of a 10% sodium carbonate solution was added the reaction mixture was heated at reflux for 1.5 h The resulting mixture was extracted with ethyl acetate the combined organic layers dried (magnesium sulfate) filtered concentrated under vacuum Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes
ソース ID: ord-3da357480ed243f08b79952da60fad6e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield. the reaction vessel purged 8 ml of a 10% sodium carbonate solution was added the reaction mixture was heated at reflux for 1.5 h The resulting mixture was extracted with ethyl acetate the combined organic layers dried (magnesium sulfate) filtered concentrated under vacuum Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes
ソース ID: ord-8bb323db14634dfba0d4059e3722cebe反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-06db46463df34a549caf9abc3aa1e02f反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-(Isopropylcarboxy)-phenylboronic acid (S. Caron and J. M. Hawkins, J. Org. Chem. 1998, 63, 2054-2055) (2.2 g, 10.6 mmol) and 2-chloro-5-trifluoromethylpyridine (500 mg, 2.75 mmol) were dissolved in toluene. Tetrakis(triphenylphosphine)palladium (160 mg, 0.14 mmol) was added and the reaction vessel purged by alternating vacuum and nitrogen gas three times. 8 ml of a 10% sodium carbonate solution was added and the reaction mixture was heated at reflux for 1.5 h. The resulting mixture was extracted with ethyl acetate, the combined organic layers dried (magnesium sulfate), filtered and concentrated under vacuum. Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes provided the title compound in approximately 70% yield. the reaction vessel purged 8 ml of a 10% sodium carbonate solution was added the reaction mixture was heated at reflux for 1.5 h The resulting mixture was extracted with ethyl acetate the combined organic layers dried (magnesium sulfate) filtered concentrated under vacuum Purification of the residue by column chromatography eluting with 10% ethyl acetate in hexanes
ソース ID: ord-3da357480ed243f08b79952da60fad6ePubChem References
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