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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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1-Butanol → Butyl Acrylate

HRID 2396401
ノート
印刷プレビュー

反応式

HRID 2396401 の反応式
[C:1]([O:5][C:6](=[O:9])[CH:7]=[CH2:8])(=O)[CH:2]=[CH2:3].[CH2:10](O)CCC>>[C:6]([O:5][CH2:1][CH2:2][CH2:3][CH3:10])(=[O:9])[CH:7]=[CH2:8]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

HCID 2631-ButanolHCID 74919Acrylic anhydride

生成物 1

HCID 8846Butyl Acrylate収率 91.2%

実験手順

According to another embodiment of the invention, the olefin acid anhydrides are reacted with alcohols to give high yields of the acrylate esters at room temperature. In particular, acrylic anhydride has been reacted with a series of alcohols ranging from C-1 to C-18 to give high yields of the acrylate esters at room temperature. The synthesis of acrylate esters by the reaction of alcohols with acrylic anhydride were found to proceed essentially to completion at room temperature to yield only the desired acrylate esters. The following mechanism is proposed for this reaction: ##STR3## No significant competing reactions were observed, such as the Michael addition reactions that often accompany the production of acrylate esters under reflux conditions. The following are representative of this embodiment: (1) the reaction of n-butyl alcohol with acrylic anhydride was completed in 3.5 hours and yielded 91.2% of n-butyl acrylate; (2) the reaction of n-octyl alcohol with acrylic anhydride was completed in 4 hours to obtain an 81.3% yield of n-octyl acrylate; and (3) the reaction of cis-12,13-epoxy-cis-9-octadecenol with acrylic anhydride was completed in 55 hours to give an 88.4% yield of cis-12, 13-epoxy-cis-9-octadecenyl acrylate.

後処理

  1. customThe following mechanism is proposed for this reaction
  2. addition##STR3## No significant competing reactions were observed, such as the Michael addition reactions that

出典と根拠

ORDレコード
ord-17fc9305388d43a484ad936e03abf614
出典データセット
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05491244

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート