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

HCID 68839044, compound → 4,6-Dihydrothieno(3,4-c)furan-1,3-dione

HRID 348062
Notes
Print preview

Reaction equation

HRID 348062 reaction equation
CO[C:3]([CH:5]1[CH2:9][S:8][CH2:7][C:6]1(O)[C:10]([OH:12])=[O:11])=[O:4]>C(OC(=O)C)(=O)C>[S:8]1[CH2:7][C:6]2[C:10]([O:12][C:3](=[O:4])[C:5]=2[CH2:9]1)=[O:11]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 68839044HCID 68839044, compound

Product 1

HCID 108881414,6-Dihydrothieno(3,4-c)furan-1,3-dioneYield 26%

Reagents, catalysts & solvents 1

HCID 7918Acetic AnhydrideSolvent

Procedure

A solution of 3-hydroxy tetrahydro thiophene-3,4-dicarboxylicacid-4-methylester (2.87 g, 14.9 mmol) in acetic anhydride (20 ml) was refluxed for 4 h. The reaction mixture was filtered and concentrated under reduce pressure. The solid residue was triturated with acetone, dried with Na2SO4 and concentrated in vacuo. The solid product was recrystallized from benzene to give 2,5-dihydrothiophene-3,4-dicarboxylic anhydride in 26% yield.

Workup

  1. filtrationThe reaction mixture was filtered
  2. concentrationconcentrated
  3. customThe solid residue was triturated with acetone
  4. dry with materialdried with Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe solid product was recrystallized from benzene

Sources & evidence

ORD record
ord-e59402433d0546e589a217e6b856568b
Source dataset
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07176241B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes