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

Diethyl Oxalate → 2,3-Quinoxalinedione, octahydro-, (4aR,8aS)-

HRID 1366656
Notes
Print preview

Reaction equation

HRID 1366656 reaction equation
[NH2:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@@H:3]1[NH2:8].[C:9](OCC)(=[O:15])[C:10](OCC)=[O:11]>COC=COC>[NH:1]1[C@@H:2]2[C@@H:3]([CH2:4][CH2:5][CH2:6][CH2:7]2)[NH:8][C:10](=[O:11])[C:9]1=[O:15]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 7268Diethyl OxalateHCID 3429171,2-Diaminocyclohexane, cis-

Product 1

HCID 574163652,3-Quinoxalinedione, octahydro-, (4aR,8aS)-Yield 66%

Reagents, catalysts & solvents 1

HCID 5223901,2-DimethoxyetheneSolvent

Conditions

Temperature
100 °C

Procedure

To a solution of cis-1,2-diaminocyclohexane (4.8 g, 42 mmol) in dimethoxy ethylene (100 mL) was added slowly diethyl oxalate (28.5 mL, 210 mmol). The reaction mixture was stirred at room temperature for 0.5 h and at 100° C. for 2 h. After the suspension was cooled down to room temperature, the resulting white solid precipitate was collected by filtration. The precipitate was washed with diethyl ether and dried to yield (4aR,8aS)-octahydro-2,3-quinoxalinedione (4.6 g, 66%). LCMS: (M+H)+: 169.1.

Workup

  1. temperatureAfter the suspension was cooled down to room temperature
  2. filtrationthe resulting white solid precipitate was collected by filtration
  3. washThe precipitate was washed with diethyl ether
  4. customdried

Sources & evidence

ORD record
ord-cb0fae6a350a40d6bffa9171db0dfa16
Source dataset
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07893056B2

Reaction notes

Loading…

On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes