反応 #4136193
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-79c49a7cbdca4bb1801f46fc104f46a1表示可能な構造データがありません
CC(COC1=CC=CC=C1)O製品情報
1-phenoxypropan-2-ol (CAS 770-35-4) 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 92839
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
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-79c49a7cbdca4bb1801f46fc104f46a1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-96765150a4e840f6b3d24fb2b5733d65反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2ec183714c754688aa2a6b139f9374e0反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-6671f0f928484bdda75d8a5c1b3147e4反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-79c49a7cbdca4bb1801f46fc104f46a1反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-79c49a7cbdca4bb1801f46fc104f46a1反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-a92c87fe015d4d3ba7d770b991676f8e反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-a92c87fe015d4d3ba7d770b991676f8e反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-6671f0f928484bdda75d8a5c1b3147e4反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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.
ソース ID: ord-6671f0f928484bdda75d8a5c1b3147e4反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-96765150a4e840f6b3d24fb2b5733d65反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-2ec183714c754688aa2a6b139f9374e0PubChem 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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