HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444537Generated: October 29, 2026
Sodium Hydroxide → HCID 131711955, compound
https://huagongshe.com/reaction/444537
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 131711952 | HCID 131711952 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131711955 | HCID 131711955 | — |
Reaction Steps
A reaction mixture was prepared containing 1.8 g. of dl-5-acetamido-1,3-di(carbomethoxy)-4,5,6,7-tetrahydro-2H-benzo[c]pyrrole, 80 ml. of THF and 20 ml. of 2 N aqueous sodium hydroxide. The reaction mixture was heated to refluxing temperature under a nitrogen atmosphere for about 3 hours after which time it was cooled and the volatile constituents evaporated therefrom in vacuo. The residue was dissolved in 25 ml. of water and the aqueous solution made acidic by the addition of 1 N aqueous hydrochloric acid. The diacid, dl-5-acetamido-1,3-dicarboxy-4,5,6,7-tetrahydro-2H-benzo[c]pyrrole, formed in the above hydrolysis being insoluble in the acidic layer precipitated and was collected by filtration. Recrystallization from a benzene-methanol solvent mixture yielded crystalline diacid melting at 233°-235° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04264622 |
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| Source dataset | uspto-grants-1981_04 |
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| ORD ID | ord-e60289b5563449e6b6ab8891fe3d346c |
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| Source note | uspto-grants-1981_04 |
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