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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604634Generated: October 30, 2026

HCID 67057700, compound → HCID 67057701, compound

https://huagongshe.com/reaction/604634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67057700HCID 67057700—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
SolventHeptaneHCID 8900—
ProductHCID 67057701HCID 67057701—

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-32981597cb1444bcbd0cb8a1a5d9fc85
Source noteuspto-grants-2011_03