反应 #4166980
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-aa1a9347db8e4dcf9f9de1c136ddb426暂无可渲染的结构数据
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4-氯苯丁酮(CAS 939-52-6)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-aa1a9347db8e4dcf9f9de1c136ddb426反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f0a5b035321447cbacf0b0445523d779反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a017e48582f84cf48213393144b96494反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-a354dee213c3409ab7834e6424297e7a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bfada7c156fe43099152b86d86a7ec10反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6396cbc657654ca7be8f5c3284f088bd反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-07f808a366434ef8b7d6d51dc7ec20ce反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-55c755485e8f40a59e400de362f80d52反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-43a22b89667342a18ad21e2a7d67853a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-530f34c610904aa7967dc1ac8abbccf6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chlorobutyrophenone (447 mg, 2.45 mmol), 4-benzamidopiperidine (500 mg, 2.45 mmol) and K2CO3 (338 mg, 2.45 mmol) was heated up in boiling water bath for 1 hour. The reaction mixture was portioned between water and CHCl3. The organic layer was separated and dried over Na2SO4. After filtration and removal of solvent, the residue was purified by chromatography (SiO2, MeOH:CHCl3, 5:95). Recrystallization from AcOEt/hexane gave a white powder (78 mg, 8.2%). mp 143-144° C.; 1H NMR (CD3OD, 400 MHz) δ1.65 (dq, J1=3.16 Hz, J2=11.9 Hz, 2H), 1.90-2.00 (m, 4H), 2.18 (t, J=11.9 Hz, 2H), 2.48 (m, 2H), 3.00-3.10 (m, 4H), 3.88 (m, 1H), 7.40-8.00 (m, 10H); Mass spectrum (M+1)+ at m/z 351. was heated up for 1 hour The organic layer was separated dried over Na2SO4 After filtration and removal of solvent the residue was purified by chromatography (SiO2, MeOH:CHCl3, 5:95) Recrystallization from AcOEt/hexane
来源 ID: ord-2c57d1872ace47f39f7aa6e63e33559d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A mixture of 4-chloro-1-phenyl-1-butanone (7.35 g) and sodium tetrahydroborate (3.05 g) in tetrahydrofuran (40 ml) was stirred for 36 h. 2M Hydrochloric acid was added and the mixture was extracted three times with ethyl acetate. The combined organic extracts were dried (magnesium sulphate), evaporated and purified by chromatography on silica eluting with petrol-ether to give the sub-title compound as a colourless oil (6.60 g). the mixture was extracted three times with ethyl acetate The combined organic extracts were dried (magnesium sulphate) evaporated purified by chromatography on silica eluting with petrol-ether
来源 ID: ord-7a8ed2afc4a345fb879f22cab26f702bPubChem References
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