書誌事項
- タイトル別名
-
- Radical Reaction of Unsaturated Acid Ester with Bromoacetonitrile
- フカン ワサン エステル ト ブロムアセトニトリル ト ノ ラジカル ハンノウ
この論文をさがす
説明
Authors studied the reactions of methyl crotonate and methyl vinylacetate with bromoacetonitrile at 120-150°C using di-tert-butylperoxide as initiator. <BR>Methyl - γ -bromocrotonate and methyl- α -bromo- β -methyl- γ -cyanobutyrate were the main products in the reaction of methyl crotonate. In case of the reaction of methyl vinylacetate, the corresponding compound (α -bromovinylacetate) was not obtained. The formation of γ -bromocrotonate in the latter case could be explained as the rearrangement of the intermediate radical CH2=CH-CHCO2CH3 into ·CH2-CH=CH-CO2CH3. <BR>Apparent activation energy of the hydrogen abstraction reaction from methyl crotonate calculated from the rate of formation of methyl- γ -bromocrotonate was lower than that from methyl vinylacetate, and apparent activation energy of the addition of bromoacetonitrile to the former was higher than that of the latter. Conjugative stabilization of intermediate radical plays an important role in theae reactions. <BR>The effect of addition of palladium chloride and of other heavy metal salts on the hydrogen ahstraction and on the addition reaction of BrCH2CN was also studied.
収録刊行物
-
- 油化学
-
油化学 15 (2), 54-58, 1966
公益社団法人 日本油化学会
- Tweet
詳細情報 詳細情報について
-
- CRID
- 1390282680310427136
-
- NII論文ID
- 130001009237
-
- NII書誌ID
- AN00245435
-
- ISSN
- 0513398X
- 18842003
-
- NDL書誌ID
- 8467221
-
- データソース種別
-
- JaLC
- NDLサーチ
- Crossref
- CiNii Articles
- OpenAIRE
-
- 抄録ライセンスフラグ
- 使用不可