HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787216Generated: October 29, 2026
HCID 86618056, compound → HCID 23114347, compound
https://huagongshe.com/reaction/1787216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86618056 | HCID 86618056 | — |
| Reactant | HCID 178418310 | HCID 178418310 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 23114347 | HCID 23114347 | 28.5% |
Reaction Steps
To a solution of ethyl (3-(4-isopropylphenyl)-4,6,7-trimethyl-2,3-dihydro-1-benzofuran-5-yl)oxamate (100 mg, 0.25 mmol) obtained in Example 15 in THF (3 ml) was added dropwise at 0° C. under an argon atmosphere tert-butylmagnesium chloride (2.0 M THF solution, 0.26 mL, 0.5 mmol) and the mixture was stirred for 30 minutes. After the reaction solution was stirred at room temperature for 1 hour, the reaction solution was added to ice and the product was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=4:1) and recrystallized from ethyl acetate-hexane to obtain 29 mg (yield: 28%) of the title compound. Melting point: 142-143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507841B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-b6d3c1a6171340e4a0e6900283c66620 |
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| Source note | uspto-grants-2009_03 |
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