反应 #4145866
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-e91703e55dd0417b969ae85a63f86073暂无可渲染的结构数据
COP(=O)(CC1=CC=C(C=C1)F)OC产品信息
1-(二甲氧基磷酰基甲基)-4-氟-苯(CAS 156745-59-4)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-e91703e55dd0417b969ae85a63f86073反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e91703e55dd0417b969ae85a63f86073反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-e91703e55dd0417b969ae85a63f86073反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 4-chloro-1-bromomethylnaphthalene is reacted with trimethylphosphite.
来源 ID: ord-d1c27e6f1c294329b349ad885927f4cf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 2-chlorobenzyl bromide is reacted with trimethylphosphite.
来源 ID: ord-bdaa62b868984ffcb14f1ad98ec1d71d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 3-fluorobenzyl bromide is reacted with trimethylphosphite.
来源 ID: ord-b75a02224a324ff892e4654d5874edf3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 2-fluorobenzyl bromide is reacted with trimethylphosphite.
来源 ID: ord-53d5bf11e10e4126b99415c1752e49d3反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 4-methylbenzyl bromide is reacted with trimethylphosphite.
来源 ID: ord-4885b845ca9047459eecdfacafc4ac38反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 3-methylbenzyl bromide is reacted with trimethylphosphite.
来源 ID: ord-d483430e27d04ed1bafcaeba34d043fc反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Following the procedure of Compound 11, 2-methylbenzyl bromide is reacted with trimethylphosphite.
来源 ID: ord-bef605dbeab649e5b17d3c663ba6b42d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-fluorobenzyl bromide (4.86 g, 0.026M) and trimethylphosphite (10 mL, 0.085M) is heated at the reflux temperature for 48 hours. The solution is cooled and excess trimethylphosphite is removed under reduced pressure. The crude product is chromatographed over silica gel (40-63 mμ, 400 g, 45 mL fractions, ethyl acetate), eluting with ethyl acetate. Fractions 41-80 are combined, concentrated, and placed under vacuum for 36 hours. The product (4.52 g) is a colorless oil. is heated at the reflux temperature for 48 hours The solution is cooled excess trimethylphosphite is removed under reduced pressure The crude product is chromatographed over silica gel (40-63 mμ, 400 g, 45 mL fractions, ethyl acetate) eluting with ethyl acetate concentrated
来源 ID: ord-55882e58f9774087b41d1694d6d8bf38反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Bromotrimethylsilane (6.0 mL, 45.4 mmol) was added dropwise to (4-fluoro-benzyl)-phosphonic acid dimethyl ester (4.57 g, 20.95 mmol) and stirred in a reaction flask chilled to 0° C. The resulting solution was allowed to warm to ambient temperature and stirred for an additional hour, then concentrated by rotary evaporation to remove volatiles yielding crude (4-fluoro-benzyl) phosphonic acid bis(trimethylsilyl) ester which was used without further purification. to warm to ambient temperature stirred for an additional hour concentrated by rotary evaporation to remove volatiles
来源 ID: ord-be9b4d6aef8942fa838ca7d8ddc153d6PubChem References
以下资料来自该化合物的公开数据库参考记录。
