反応 #4145807
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-483d736541bb4fb09782752c059df177表示可能な構造データがありません
CCO[Si](OCC)(OCC)Cl製品情報
chloro(triethoxy)silane (CAS 4667-99-6) 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 78398
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-483d736541bb4fb09782752c059df177反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-31bfc7375748486298b645cd632617c5反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 15.246 g (0.10 mol) sodium chlorodifluoroacetate, is dissolved to 100 mL Et2O and cooled to −70° C. 19.7 mL (0.10 mol, 19.872 g) chlorotriethoxysilane in Et2O (50 mL) was added dropwise to reaction solution. The solution was stirred for over night allowing it to warm up to room temperature. NaCl is removed by filtration and solution evaporated to dryness to result clear colourless liquid, chlorodifluoroacetic acid, triethoxysilyl ester. to warm up to room temperature NaCl is removed by filtration and solution evaporated to dryness
ソース ID: ord-952c4637cec247c382f31cb28c094e32反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 6.123 g (0.0651 mol) sodium acrylate is dissolved to 25 mL THF and cooled to −70° C. 12.8 mL (0.0651 mol, 12.938 g) chlorotriethoxysilane in THF (15 mL) is added dropwise to reaction solution. The solution is stirred for over night allowing it to warm up to room temperature. NaCl is removed by filtration and solution evaporated to dryness to result clear liquid, acryltriethoxysilane. to warm up to room temperature NaCl is removed by filtration and solution evaporated to dryness
ソース ID: ord-beaf8c195b974115996103f04de0333c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-483d736541bb4fb09782752c059df177反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-483d736541bb4fb09782752c059df177反応条件: temp:23.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Chlorotriethoxysilane (2.0 mL, 10 mmol, 1.0 equiv) was added to a stirred solution of 0.5M ethynylmagnesium bromide (20 mL, 10 mmol, 1.0 equiv) in tetrahydrofuran (10 mL) at −78° C. The resulting heterogeneous light brown mixture was immediately warmed to 23° C. and stirred for 1 h. The resulting homogeneous light brown solution was heated to 50° C. and stirred for 4 h. The cooled reaction mixture was concentrated under vacuum. The resulting tan powder was slurried in hexane (50 mL), vacuum filtered, and rinsed with additional hexane (3×25 mL). The filtrates were dried over magnesium sulfate, gravity filtered, and concentrated under vacuum to provide the title compound as a pale yellow oil (1.5 g, 80% yield): IR (thin film) 3252 (w), 2976 (s), 2929 (m), 2913 (w), 2890 (m), 2046 (m) cm−1; 1H NMR (400 MHz, CDCl3) δ 3.90 (q, J=7 Hz, 6H), 2.35 (s, 1H), 1.23 (t, J=7 Hz, 9H). The resulting homogeneous light brown solution was heated to 50° C. stirred for 4 h The cooled reaction mixture was concentrated under vacuum vacuum filtered rinsed with additional hexane (3×25 mL) The filtrates were dried over magnesium sulfate, gravity filtered concentrated under vacuum
ソース ID: ord-478d6e4e44144b7fa5cf2ef8b91e555a反応条件: temp:23.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Chlorotriethoxysilane (2.0 mL, 10 mmol, 1.0 equiv) was added to a stirred solution of 0.5M ethynylmagnesium bromide (20 mL, 10 mmol, 1.0 equiv) in tetrahydrofuran (10 mL) at −78° C. The resulting heterogeneous light brown mixture was immediately warmed to 23° C. and stirred for 1 h. The resulting homogeneous light brown solution was heated to 50° C. and stirred for 4 h. The cooled reaction mixture was concentrated under vacuum. The resulting tan powder was slurried in hexane (50 mL), vacuum filtered, and rinsed with additional hexane (3×25 mL). The filtrates were dried over magnesium sulfate, gravity filtered, and concentrated under vacuum to provide the title compound as a pale yellow oil (1.5 g, 80% yield): IR (thin film) 3252 (w), 2976 (s), 2929 (m), 2913 (w), 2890 (m), 2046 (m) cm−1; 1H NMR (400 MHz, CDCl3) δ 3.90 (q, J=7 Hz, 6H), 2.35 (s, 1H), 1.23 (t, J=7 Hz, 9H). The resulting homogeneous light brown solution was heated to 50° C. stirred for 4 h The cooled reaction mixture was concentrated under vacuum vacuum filtered rinsed with additional hexane (3×25 mL) The filtrates were dried over magnesium sulfate, gravity filtered concentrated under vacuum
ソース ID: ord-478d6e4e44144b7fa5cf2ef8b91e555a反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 15.246 g (0.10 mol) sodium chlorodifluoroacetate, is dissolved to 100 mL Et2O and cooled to −70° C. 19.7 mL (0.10 mol, 19.872 g) chlorotriethoxysilane in Et2O (50 mL) was added dropwise to reaction solution. The solution was stirred for over night allowing it to warm up to room temperature. NaCl is removed by filtration and solution evaporated to dryness to result clear colourless liquid, chlorodifluoroacetic acid, triethoxysilyl ester. to warm up to room temperature NaCl is removed by filtration and solution evaporated to dryness
ソース ID: ord-52cd7162f55e4d0cbcb0f72367c04508反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 6.123 g (0.0651 mol) sodium acrylate is dissolved to 25 mL THF and cooled to −70° C. 12.8 mL (0.0651 mol, 12.938 g) chlorotriethoxysilane in THF (15 mL) is added dropwise to reaction solution. The solution is stirred for over night allowing it to warm up to room temperature. NaCl is removed by filtration and solution evaporated to dryness to result clear liquid, acryltriethoxysilane. to warm up to room temperature NaCl is removed by filtration and solution evaporated to dryness
ソース ID: ord-5246108e8bdd422b967754ebf688e510反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 15.246 g (0.10 mol) sodium chlorodifluoroacetate, is dissolved to 100 mL Et2O and cooled to −70° C. 19.7 mL (0.10 mol, 19.872 g) chlorotriethoxysilane in Et2O (50 mL) was added dropwise to reaction solution. The solution was stirred for over night allowing it to warm up to room temperature. NaCl is removed by filtration and solution evaporated to dryness to result clear colourless liquid, chlorodifluoroacetic acid, triethoxysilyl ester. to warm up to room temperature NaCl is removed by filtration and solution evaporated to dryness
ソース ID: ord-4ab5667fd8684b8ba74f5b1fcfa3c07e反応条件: temp:-70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 15.246 g (0.10 mol) sodium chlorodifluoroacetate, is dissolved to 100 mL Et2O and cooled to −70° C. 19.7 mL (0.10 mol, 19.872 g) chlorotriethoxysilane in Et2O (50 mL) was added dropwise to reaction solution. The solution was stirred for over night allowing it to warm up to room temperature. NaCl is removed by filtration and solution evaporated to dryness to result clear colourless liquid, chlorodifluoroacetic acid, triethoxysilyl ester. to warm up to room temperature NaCl is removed by filtration and solution evaporated to dryness
ソース ID: ord-4ab5667fd8684b8ba74f5b1fcfa3c07ePubChem References
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