Fumarate → bromomesaconic acid
反応式
[Br:1][CH2:2]/[C:3](=[CH:7]/[C:8]([OH:10])=[O:9])/[C:4]([OH:6])=[O:5].C([O-])(=O)/C=C/C([O-])=O.BrCC1C(OC(=O)C=1)=O>>[Br:1][CH2:2]/[C:3](=[CH:7]\[C:8]([OH:10])=[O:9])/[C:4]([OH:6])=[O:5]参加物
4
実験手順
Steps are taken to avoid isomerization of 2-(bromomethyl)-maleic acid (3) to the corresponding fumarate analog by hydrolyzing the anhydride (2) in a dilute aqueous solution and neutralizing the diacid (3) immediately after complete hydrolysis. Any bromomethyl fumaric acid derivative formed is removed in purifying compound (4) as described in more detail below.
後処理
- customimmediately after complete hydrolysis
出典と根拠
- ORDレコード
- ord-ac773b44e71f4e68b80f6832a35f9a2e
- 出典データセット
- uspto-grants-1986_10
- 特許番号
- US04618492
反応ノート
読み込み中…