HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604634Generated: October 30, 2026
HCID 67057700, compound → HCID 67057701, compound
https://huagongshe.com/reaction/604634
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 67057700 | HCID 67057700 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | HCID 67057701 | HCID 67057701 | — |
Reaction Steps
To a solution of methyl 6-(4-fluoro-5-isopropyl-2-methoxyphenyl)-3-oxoindane-5-carboxylate (45.9 mg, 0.129 mmol) in heptane (1 mL) and THF (1 mL) at −20° C. under N2, was added dropwise 3N MeMgCl in THF (86 uL, 0.258 mmol). The reaction mixture was stirred at −20° C. for 2 h. The mixture was quenched with sat. aq. NH4Cl and extracted with EtOAc (3×). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel to give methyl 6-(4-fluoro-5-isopropyl-2-methoxyphenyl)-3-hydroxy-3-methylindane-5-carboxylate. LCMS calc.=395.2; found=394.9 (M+Na)+. 1H NMR (500 MHz, CDCl3): δ 7.89 (s, 1H); 7.20 (s, 1H); 7.09 (d, J=8.6 Hz, 1H); 6.62 (d, J=12.1 Hz, 1H); 3.72 (s, 3H); 3.70 (s, 3H); 3.28-3.20 (m, 1H); 3.15-3.09 (m, 1H); 2.96-2.90 (m, 1H); 2.36-2.24 (m, 2H); 1.91 (br s, 1H); 1.66 (s, 3H); 1.30 (d, J=6.9 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910592B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-32981597cb1444bcbd0cb8a1a5d9fc85 |
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| Source note | uspto-grants-2011_03 |
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