HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277601Generated: October 30, 2026
Boron trifluoride etherate → HCID 84732417, compound
https://huagongshe.com/reaction/2277601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86685928 | HCID 86685928 | — |
| Reactant | HCID 86685929 | HCID 86685929 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-2,3-dihydro-3-methyl-1H-isoindol-1-one | HCID 84732416 | 9.6% |
| Product | HCID 84732417 | HCID 84732417 | 11% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133158B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-88c7f1e9b6ae42a2923650cd45745ea9 |
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| Source note | uspto-grants-2015_09 |
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