オキシアルデヒドの合成的研究(第1報) : 芳香族ニトロ化合物による酸化に就いて
書誌事項
- タイトル別名
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- オキシアルデヒド ノ ゴウセイテキ ケンキュウ (ダイ1ポウ) : ホウコウゾク ニトロ カゴウブツ ニ ヨル サンカ ニ ツイテ
- Okishiarudehido no goseiteki kenkyu (dai1po) : hokozoku nitoro kagobutsu ni yoru sanka ni tsuite
- On the synthetic investigation of oxy-aldehyd (1), about oxydation by the aromatic nitro compounds
説明
type:text
The oxidation of p-oxybenzylalcohol into p-oxybenzaldehyd was investigated. Many aromatic nitro compounds nitrobenzene, nitrophenols, chloronitrobenzenes, dinitrobenzenes, nitrobenzoic acids, and nitrobenzene sulfonic acids-were used as oxidizing reagents. The alkali solution of p-oxybenzylalcohol and the aromatic nitro compound was heated under the reflux condenser about 3hrs, and the yield of p-oxybenzaldehyd estimated by the hydroxylamin method. I came to the conclusions as follows: 1) Generally, the more negative the substituted radical of the aromatic nitro compound is, the higher the yield of p-oxybenzaldehyd. 2) Among o-, p-, and m-isomer, the last gave highest yield. 3) I considered D ((2) and Table 6) as a potency of activity of nitro radical, and could express the relation between D and log X (X: the yield of p-oxybenzaldehyd) with the linear equation (4).
収録刊行物
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- 慶應義塾大学藤原記念工学部研究報告
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慶應義塾大学藤原記念工学部研究報告 2 (4), 35(35)-40(40), 1949-04
慶應義塾大学藤原記念工学部
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詳細情報 詳細情報について
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- CRID
- 1050845763880846976
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- NII論文ID
- 120005479299
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- 本文言語コード
- ja
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- 資料種別
- departmental bulletin paper
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- データソース種別
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- IRDB
- CiNii Articles