反応 #4175081
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-41c8d74a2f24456bbbc2999ccf31a7cb表示可能な構造データがありません
COCCCO製品情報
3-methoxypropan-1-ol (CAS 1589-49-7) 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 74116
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-41c8d74a2f24456bbbc2999ccf31a7cb反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6a0122fb7141473ca9531302ae9c3e45反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b6ebedc381214213b9b7648aae235c3c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9a9e4b6f3ceb4bfa87dfd445d06a156b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-03201b088ecd4a4c84f6aa0295a5b335反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-43e7a1f4426540f69a855fdd114cbb28反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-90819cf78c5a49e9b888eef14b5de7cb反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-c788234ad48440049ada1e5f2306085e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-e68da358cdd44488a1d3cf44011fd83d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-5d9497b215574fdc9063a255efce5064反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-0c7d43132de04827af020fd341883583反応条件: temp:0.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: A solution of 3-methoxypropan-1-ol [Fluka product #38457] (3.1 mL, 32 mmol) and triphenylphosphine (8.4 g, 32 mmol) in tetrahydrofuran (93 mL) at 0° C. was treated with diisopropyl azodicarboxylate (6.7 mL, 34 mmol) dropwise. The reaction mixture was stirred at 0° C. for 15 min, treated with a solution of N-{4-[4-(3-bromo-4-fluorophenyl)-5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl]-1,2,5-oxadiazol-3-yl}-2,2,2-trifluoroacetamide (10 g, 23 mmol) in tetrahydrofuran (47 mL), and stirred at 25° C. for 72 h. The reaction mixture was concentrated, diluted with ethyl acetate (200 mL), treated with trifluoroacetic acid (20 mL) and water (20 mL), and heated at 50° C. for 6 h. The reaction mixture was concentrated, rediluted with ethyl acetate (200 mL) and washed with water (3×80 mL), saturated sodium bicarbonate (2×80 mL) and brine (80 mL), dried over anhydrous sodium sulfate, filtered, and concentrated to a crude residue. This material was purified on silica gel to give the desired product (6.4 g, 54%) as a white solid. LCMS for C14H14BrFN5O4 (M+H)+: m/z=414.0, 416.0. stirred at 25° C. for 72 h The reaction mixture was concentrated diluted with ethyl acetate (200 mL) treated with trifluoroacetic acid (20 mL) and water (20 mL) heated at 50° C. for 6 h The reaction mixture was concentrated rediluted with ethyl acetate (200 mL) washed with water (3×80 mL), saturated sodium bicarbonate (2×80 mL) and brine (80 mL) dried over anhydrous sodium sulfate filtered concentrated to a crude residue This material was purified on silica gel
ソース ID: ord-d424ea94f0254c7c83223bbfbd754a39PubChem 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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