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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277601Generated: October 30, 2026

Boron trifluoride etherate → HCID 84732417, compound

https://huagongshe.com/reaction/2277601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86685928HCID 86685928—
ReactantHCID 86685929HCID 86685929—
SolventDichloromethaneHCID 6344—
Product6-Chloro-2,3-dihydro-3-methyl-1H-isoindol-1-oneHCID 847324169.6%
ProductHCID 84732417HCID 8473241711%

Reaction Steps

Under N2 protection, triethylsilane (23 g, 200 mmol) and trifluoroboron etherate (8.51 g, 60 mmol) were added successively at −15° C. to a mixture of 5-chloro-3-hydroxy-3-methyl-2,3-dihydro-isoindol-1-one and 6-chloro-3-hydroxy-3-methyl-2,3-dihydro-isoindol-1-one (3.95 g, 20 mmol) in dry DCM (100 mL). Afterwards, the reaction mixture was stirred at room temperature for 2 hours and a saturated aqueous solution of NaHCO3 (30 mL) was added. The mixture was then extracted with DCM and the organic layer was washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo to give a crude mixture of products. The two regioisomers were separated by prep-HPLC to give the title compounds, 5-chloro-3-methyl-2,3-dihydro-isoindol-1-one (0.4 g, 11%) and 6-chloro-3-methyl-2,3-dihydro-isoindol-1-one (0.35 g, 9.6%) as white solids. MS: 182.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133158B2
Source datasetuspto-grants-2015_09
ORD IDord-88c7f1e9b6ae42a2923650cd45745ea9
Source noteuspto-grants-2015_09