反应 #4136193
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-79c49a7cbdca4bb1801f46fc104f46a1暂无可渲染的结构数据
CC(COC1=CC=CC=C1)O产品信息
1-苯氧基-2-丙醇(CAS 770-35-4)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 92839
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-79c49a7cbdca4bb1801f46fc104f46a1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-96765150a4e840f6b3d24fb2b5733d65反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2ec183714c754688aa2a6b139f9374e0反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The present invention is directed to an antimicrobial composition and a method of using said composition, comprising an antimicrobially effective amount of DTEA and an amount of 1-butanol, cyclohexanol, hexyl alcohol, isobutanol, ethylene glycol phenyl ether, propylene glycol phenyl ether, or a mixture thereof effective to result in the antimicrobial composition having a freezing point of less than 0° C. at atmospheric pressure.
来源 ID: ord-6671f0f928484bdda75d8a5c1b3147e4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-79c49a7cbdca4bb1801f46fc104f46a1反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-79c49a7cbdca4bb1801f46fc104f46a1反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phenoxy-2-propanone (3.4 mL, 25 mmol) was dissolved in ethanol (30 mL) and cooled to 0° C. Sodium borohydride (0.95 g; 25 mmol; 1 equiv.) was added. The mixture was stirred and allowed to warm to room temperature overnight. All of the starting material was gone according to tlc analysis, so the mixture was poured into water (30 mL) and ether (30 mL). The layers were separated and the aqueous layer was extracted with ether (2×20 mL). The organic layers were combined and concentrated. The resulting aqueous residue was poured into ether (25 mL). The organic layer was removed, dried (MgSO4), and concentrated to provide 1e (3.2 g; 85%). 1H nmr (300 MHz, CDCl3): 7.332-7.261 (3H, m); 6.995-6.904 (2H, m); 4.15-4.24 (1H, m); 3.972-3.768 (2H, m); 1.559 (1H, s); 1.290 (3H, d, J=6.38 Hz). IR (neat film, cm-1): 3350 (b, s); 2900 (s); 1590 (m). EIMS (m/e): 152 (M+). to warm to room temperature overnight The layers were separated the aqueous layer was extracted with ether (2×20 mL) concentrated The resulting aqueous residue was poured into ether (25 mL) The organic layer was removed dried (MgSO4) concentrated
来源 ID: ord-a92c87fe015d4d3ba7d770b991676f8e反应条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Phenoxy-2-propanone (3.4 mL, 25 mmol) was dissolved in ethanol (30 mL) and cooled to 0° C. Sodium borohydride (0.95 g; 25 mmol; 1 equiv.) was added. The mixture was stirred and allowed to warm to room temperature overnight. All of the starting material was gone according to tlc analysis, so the mixture was poured into water (30 mL) and ether (30 mL). The layers were separated and the aqueous layer was extracted with ether (2×20 mL). The organic layers were combined and concentrated. The resulting aqueous residue was poured into ether (25 mL). The organic layer was removed, dried (MgSO4), and concentrated to provide 1e (3.2 g; 85%). 1H nmr (300 MHz, CDCl3): 7.332-7.261 (3H, m); 6.995-6.904 (2H, m); 4.15-4.24 (1H, m); 3.972-3.768 (2H, m); 1.559 (1H, s); 1.290 (3H, d, J=6.38 Hz). IR (neat film, cm-1): 3350 (b, s); 2900 (s); 1590 (m). EIMS (m/e): 152 (M+). to warm to room temperature overnight The layers were separated the aqueous layer was extracted with ether (2×20 mL) concentrated The resulting aqueous residue was poured into ether (25 mL) The organic layer was removed dried (MgSO4) concentrated
来源 ID: ord-a92c87fe015d4d3ba7d770b991676f8e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The present invention is directed to an antimicrobial composition and a method of using said composition, comprising an antimicrobially effective amount of DTEA and an amount of 1-butanol, cyclohexanol, hexyl alcohol, isobutanol, ethylene glycol phenyl ether, propylene glycol phenyl ether, or a mixture thereof effective to result in the antimicrobial composition having a freezing point of less than 0° C. at atmospheric pressure.
来源 ID: ord-6671f0f928484bdda75d8a5c1b3147e4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The present invention is directed to an antimicrobial composition and a method of using said composition, comprising an antimicrobially effective amount of DTEA and an amount of 1-butanol, cyclohexanol, hexyl alcohol, isobutanol, ethylene glycol phenyl ether, propylene glycol phenyl ether, or a mixture thereof effective to result in the antimicrobial composition having a freezing point of less than 0° C. at atmospheric pressure.
来源 ID: ord-6671f0f928484bdda75d8a5c1b3147e4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-96765150a4e840f6b3d24fb2b5733d65反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2ec183714c754688aa2a6b139f9374e0PubChem References
以下资料来自该化合物的公开数据库参考记录。
相关产品
12 related records
CAS 622-62-8
CAS 5349-18-8
CAS 2212-05-7
CAS 2460-87-9
CAS 18181-71-0
CAS 18979-55-0
CAS 4812-20-8
CAS 493-09-4
CAS 147825-65-8
CAS 2212-06-8
CAS 33426-69-6
CAS 71031-03-3
