反応 #4160626
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-63e79551e80d4af7b897d4b3ce5e8297表示可能な構造データがありません
CC(C)CCCC(C)CCBr製品情報
1-bromo-3,7-dimethyloctane (CAS 3383-83-3) 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 137914
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-63e79551e80d4af7b897d4b3ce5e8297反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ee246d1adb0146cf9b79f4334c85f78c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f6559edc63194477912bdcdaf35f0c30反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-66cc9cd1b41e4c85a76859ae813e60c3反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-1a629a0b836a4ac283d0549c3db89b9d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-9dbd1e74ca6644d482399f414ec8b87e反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f618cb57b29c4d1ba047886dfab05814反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-63e79551e80d4af7b897d4b3ce5e8297反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-ee246d1adb0146cf9b79f4334c85f78c反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-f6559edc63194477912bdcdaf35f0c30反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Under an inert atmosphere, 90 g of 3-bromophenol was dissolved in 600 ml of ethanol. Further, 39 g potassium hydroxide was added to this and the mixture was heated up to 70° C. for dissolution thereof. From a dropping funnel, 126 g of 3,7-dimethylbromooctane was dropped over 15 minutes. After completion of dropping, the mixture was heated to 84° C. and stirred for about 22 hours under heat. After completion of heating, the mixture was left to cool to room temperature. The reaction solution was bisected, 500 ml of water was added to respective portions, then, ethanol was distilled off by an evaporator. The solutions after distilling off of ethanol were combined and trisected, 300 ml of ethyl acetate was added to respective portions to cause liquid separation, and the organic layers were washed with 200 ml of water twice. The organic layers were combined and the solvent was distilled off by an evaporator, then, the residue was dried by heating at 90° C. for 5 hours under vacuum by a rotary pump. About 150 g of 3-(3,7-dimethyloctyloxy)-bromobenzene was obtained as an oily product. the mixture was heated to 84° C. under heat After completion of heating the mixture was left to cool to room temperature ethanol was distilled off by an evaporator The solutions after distilling off of ethanol 300 ml of ethyl acetate was added to respective portions liquid separation the organic layers were washed with 200 ml of water twice the solvent was distilled off by an evaporator the residue was dried by heating at 90° C. for 5 hours under vacuum by a rotary pump
ソース ID: ord-6ae149b736fd429585295ac1c36f5e49反応条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: Under an inert atmosphere, 90 g of 3-bromophenol was dissolved in 600 ml of ethanol. Further, 39 g potassium hydroxide was added to this and the mixture was heated up to 70° C. for dissolution thereof. From a dropping funnel, 126 g of 3,7-dimethylbromooctane was dropped over 15 minutes. After completion of dropping, the mixture was heated to 84° C. and stirred for about 22 hours under heat. After completion of heating, the mixture was left to cool to room temperature. The reaction solution was bisected, 500 ml of water was added to respective portions, then, ethanol was distilled off by an evaporator. The solutions after distilling off of ethanol were combined and trisected, 300 ml of ethyl acetate was added to respective portions to cause liquid separation, and the organic layers were washed with 200 ml of water twice. The organic layers were combined and the solvent was distilled off by an evaporator, then, the residue was dried by heating at 90° C. for 5 hours under vacuum by a rotary pump. About 150 g of 3-(3,7-dimethyloctyloxy)-bromobenzene was obtained as an oily product. the mixture was heated to 84° C. under heat After completion of heating the mixture was left to cool to room temperature ethanol was distilled off by an evaporator The solutions after distilling off of ethanol 300 ml of ethyl acetate was added to respective portions liquid separation the organic layers were washed with 200 ml of water twice the solvent was distilled off by an evaporator the residue was dried by heating at 90° C. for 5 hours under vacuum by a rotary pump
ソース ID: ord-6ae149b736fd429585295ac1c36f5e49PubChem 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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