反応 #4166980
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-aa1a9347db8e4dcf9f9de1c136ddb426表示可能な構造データがありません
C1=CC=C(C=C1)C(=O)CCCCl製品情報
4-chloro-1-phenylbutan-1-one (CAS 939-52-6) 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 253533
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-aa1a9347db8e4dcf9f9de1c136ddb426反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f0a5b035321447cbacf0b0445523d779反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a017e48582f84cf48213393144b96494反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-a354dee213c3409ab7834e6424297e7a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-bfada7c156fe43099152b86d86a7ec10反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-6396cbc657654ca7be8f5c3284f088bd反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-07f808a366434ef8b7d6d51dc7ec20ce反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-55c755485e8f40a59e400de362f80d52反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-43a22b89667342a18ad21e2a7d67853a反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-530f34c610904aa7967dc1ac8abbccf6反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-2c57d1872ace47f39f7aa6e63e33559d反応条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 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
ソース ID: ord-7a8ed2afc4a345fb879f22cab26f702bPubChem 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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