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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactantmethyl 1-oxo-2,3-dihydro-1H-isoindole-5-carboxylateHCID 69114316—
SolventWaterHCID 962—
Product1-Oxo-2,3-dihydro-1H-isoindole-5-carboxylic acidHCID 12850266—

Reaction Conditions

Temperature23 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096527B2
Source datasetuspto-grants-2015_08
ORD IDord-8e2647b000154c8799f46eb4f3e6755e
Source noteuspto-grants-2015_08