HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Potassium Hydroxide → 2-(4-Bromobenzyl)malonic acid

HRID 1503367
Notes
Print preview

Reaction equation

HRID 1503367 reaction equation
[Br:1][C:2]1[CH:19]=[CH:18][C:5]([CH2:6][CH:7]([C:13]([O:15]CC)=[O:14])[C:8]([O:10]CC)=[O:9])=[CH:4][CH:3]=1.[OH-].[K+]>OC(C)=O.O.C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][CH:7]([C:8]([OH:10])=[O:9])[C:13]([OH:15])=[O:14])=[CH:18][CH:19]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 14797Potassium HydroxideHCID 10860456Diethyl 2-(4-bromobenzyl)malonate

Product 1

HCID 133302152-(4-Bromobenzyl)malonic acidYield 873.2%

Reagents, catalysts & solvents 1

HCID 21877175AcOH THF waterSolvent

Procedure

Diethyl 2-(4-bromobenzyl)malonate (40 g, 13 mmol) and KOH (42.8 g, 76 mmol) was dissolved in a mixture of HOAc—H2O-THF (1:2:3, 200 mL), the mixture was refluxed for 12 hours. The solvent was removed in vacuo, the residue was added HCl aqueous, then extracted with EtOAc, washed with brine, dried over Na2SO4, concentrated to give 2-(4-bromobenzyl)malonic acid (31 g, 95%).

Workup

  1. temperaturethe mixture was refluxed for 12 hours
  2. customThe solvent was removed in vacuo
  3. additionthe residue was added HCl aqueous
  4. extractionextracted with EtOAc
  5. washwashed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-f1f8d2fac8d84fe1aee24a9aab0bc51f
Source dataset
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09212153B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes