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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1511537Generated: November 3, 2026

Hydrochloric Acid → 4-Chloro-2,3-dihydro-1H-isoindole

https://huagongshe.com/reaction/1511537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant4-chloroisoindole-1,3-dioneHCID 231238—
ReactantBorane;tetrahydrofuranHCID 2723981—
Product4-Chloro-2,3-dihydro-1H-isoindoleHCID 1479586853.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To solid 4-chloro-1H-isoindole-1,3(2H)-dione (4.0 g, 22.0 mmol) was added borane-THF complex (1 M/THF, 88.1 mL, 88.1 mmol) dropwise with stirring. When the addition was complete, the reaction mixture was heated to reflux (80° C.) and stirred for 6 h. The reaction mixture was then cooled to 0° C., methanol (2.8 mL, 88.1 mmol) was carefully added dropwise and the reaction mixture was warmed to room temperature. HCl (6 N) was added until the mixture was acidic and then the mixture was concentrated. The crude product was dissolved in 1 M HCl and extracted twice with ethyl ether and twice with dichloromethane. The pH of the aqueous layer was adjusted to pH=11 with solid NaOH and extracted three times with ethyl acetate. The combined ethyl acetate extracts were dried over Na2SO4, filtered and concentrated to give 4-chloroisoindoline (1.8 g, 53% yield). LRMS (ESI) m/z 154 [(M+H)+; calcd for C8H9ClN: 154].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08216999B2
Source datasetuspto-grants-2012_07
ORD IDord-03abb9b00284400fbc463bc7e693f964
Source noteuspto-grants-2012_07