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

Ammonia → Methoxymalonamic acid

HRID 1493083
Notes
Print preview

Reaction equation

HRID 1493083 reaction equation
[CH3:1][O:2][CH:3]([C:8]([O-:10])=O)[C:4]([O:6]C)=[O:5].[NH3:11]>C(Cl)Cl>[CH3:1][O:2][CH:3]([C:8]([NH2:11])=[O:10])[C:4]([OH:6])=[O:5]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 222AmmoniaHCID 229990802,3-Dimethoxy-3-oxopropanoate

Product 1

HCID 19373134Methoxymalonamic acid

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A solution of 10.4 g of monomethyl methoxymalonate in 70 ml of methylene chloride was added dropwise at -10° C. to 26 ml of 25 percent aqueous ammonia. After stirring the mixture was evaporated and the residue was dissolved in water and chromato- graphed on a cation exchanger with water. The eluate was concentrated and the residue was triturated with diethyl ether and filtered off. The precipitate was washed with water and dried. There were obtained 8.9 g of methoxymalonamic acid, m.p. 128°-130° C.

Workup

  1. customwas evaporated
  2. dissolutionthe residue was dissolved in water
  3. concentrationThe eluate was concentrated
  4. customthe residue was triturated with diethyl ether
  5. filtrationfiltered off
  6. washThe precipitate was washed with water
  7. customdried

Sources & evidence

ORD record
ord-e16920443b9b4263be70fc9518178798
Source dataset
uspto-grants-1994_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05376674

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes