反应 #4144858
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-93ce31075ee846349638060ac37fe88a暂无可渲染的结构数据
COC1=C(C=CC(=C1)CO)N产品信息
4-氨基-3-甲氧基苯甲醇(CAS 148459-54-5)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-93ce31075ee846349638060ac37fe88a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0b032757978b490db5d8e9fa55b96195反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-93ce31075ee846349638060ac37fe88a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-93ce31075ee846349638060ac37fe88a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-amino-3-methoxybenzyl alcohol (900 mg) in methanol was added acetic anhydride (1.8 g) under ice cooling, and the mixture was stirred for 1 hour at the same temperature. After evaporation, the residue was dissolved in ethyl acetate, and the solution was washed with sodium bicarbonate solution, water and brine, dried over magnesium sulfate and concentrated in vacuo to give 4-acetamido-3-methoxybenzyl alcohol (840 mg) as solid. After evaporation the residue was dissolved in ethyl acetate the solution was washed with sodium bicarbonate solution, water and brine dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-5714f59fa6e141db99194845b6bd21bd反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 3-methoxy-4-nitrobenzyl alcohol (1.0 g) and 10% palladium on carbon (100 mg) in methanol was stirred for 2 hours under 3 atmospheric pressure of hydrogen. After filtration, the filtrate was concentrated in vacuo to give 4-amino-3-methoxybenzyl alcohol (910 mg) as an oil. After filtration the filtrate was concentrated in vacuo
来源 ID: ord-9a0de115e331445b82d099de9e24117a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 3-methoxy-4-nitrobenzyl alcohol (1.0 g) and 10% palladium on carbon (100 mg) in methanol was stirred for 2 hours under 3 atmospheric pressure of hydrogen. After filtration, the filtrate was concentrated in vacuo to give 4-amino-3-methoxybenzyl alcohol (910 mg) as an oil. After filtration the filtrate was concentrated in vacuo
来源 ID: ord-9a0de115e331445b82d099de9e24117a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-amino-3-methoxybenzyl alcohol (900 mg) in methanol was added acetic anhydride (1.8 g) under ice cooling, and the mixture was stirred for 1 hour at the same temperature. After evaporation, the residue was dissolved in ethyl acetate, and the solution was washed with sodium bicarbonate solution, water and brine, dried over magnesium sulfate and concentrated in vacuo to give 4-acetamido-3-methoxybenzyl alcohol (840 mg) as solid. After evaporation the residue was dissolved in ethyl acetate the solution was washed with sodium bicarbonate solution, water and brine dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-8912a1a0b9424178a4edcdf5a886c8e5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-amino-3-methoxybenzyl alcohol (900 mg) in methanol was added acetic anhydride (1.8 g) under ice cooling, and the mixture was stirred for 1 hour at the same temperature. After evaporation, the residue was dissolved in ethyl acetate, and the solution was washed with sodium bicarbonate solution, water and brine, dried over magnesium sulfate and concentrated in vacuo to give 4-acetamido-3-methoxybenzyl alcohol (840 mg) as solid. After evaporation the residue was dissolved in ethyl acetate the solution was washed with sodium bicarbonate solution, water and brine dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-8912a1a0b9424178a4edcdf5a886c8e5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 3-methoxy-4-nitrobenzyl alcohol (1.0 g) and 10% palladium on carbon (100 mg) in methanol was stirred for 2 hours under 3 atmospheric pressure of hydrogen. After filtration, the filtrate was concentrated in vacuo to give 4-amino-3-methoxybenzyl alcohol (910 mg) as an oil. After filtration the filtrate was concentrated in vacuo
来源 ID: ord-91bce1332ac54aae9e0c19f0f9b55334反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-0b032757978b490db5d8e9fa55b96195反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a solution of 4-amino-3-methoxybenzyl alcohol (900 mg) in methanol was added acetic anhydride (1.8 g) under ice cooling, and the mixture was stirred for 1 hour at the same temperature. After evaporation, the residue was dissolved in ethyl acetate, and the solution was washed with sodium bicarbonate solution, water and brine, dried over magnesium sulfate and concentrated in vacuo to give 4-acetamido-3-methoxybenzyl alcohol (840 mg) as solid. After evaporation the residue was dissolved in ethyl acetate the solution was washed with sodium bicarbonate solution, water and brine dried over magnesium sulfate concentrated in vacuo
来源 ID: ord-5714f59fa6e141db99194845b6bd21bdPubChem References
以下资料来自该化合物的公开数据库参考记录。
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