Fumarate → bromomesaconic acid
Reaction equation
[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]Participants
4
Procedure
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.
Workup
- customimmediately after complete hydrolysis
Sources & evidence
- ORD record
- ord-ac773b44e71f4e68b80f6832a35f9a2e
- Source dataset
- uspto-grants-1986_10
- Patent number
- US04618492
Reaction notes
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