HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509353Generated: October 26, 2026
Hydrochloric Acid → 1-Oxo-2,3-dihydro-1H-isoindole-5-carboxylic acid
https://huagongshe.com/reaction/509353
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | methyl 1-oxo-2,3-dihydro-1H-isoindole-5-carboxylate | HCID 69114316 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Oxo-2,3-dihydro-1H-isoindole-5-carboxylic acid | HCID 12850266 | — |
Reaction Steps
To a 100 mL round bottom flask containing methyl 1-oxoisoindoline-5-carboxylate (200 mg, 1.046 mmol) was added THF (6 mL) and H2O (2 mL) the mixture was stirred at 23° C. for 2 min. At this time, lithium hydroxide monohydrate (87 μL, 3.14 mmol) was added and the flask was gently heated on aluminum block for 5 min. The solid went into solution and LC/MS showed product formation. The contents of the reaction were poured into HCl (1 M, 15 mL) and extracted with DCM (15 mL). An emulsion formed, the layers separated, and a white solid formed at the boundary of the layers and stuck to the separatory funnel. This material was collected, dissolved in MeOH, and concentrated. After drying under high vacuum for 2 h, the 1-oxoisoindoline-5-carboxylic acid thus obtained was taken on directly to the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096527B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-8e2647b000154c8799f46eb4f3e6755e |
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| Source note | uspto-grants-2015_08 |
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