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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604635Generated: October 29, 2026

p-Toluenesulfonic acid → HCID 67057742, compound

https://huagongshe.com/reaction/604635

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantHCID 67057701HCID 67057701—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 67057742HCID 67057742—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 6-(4-fluoro-5-isopropyl-2-methoxyphenyl)-3-hydroxy-3-methylindane-5-carboxylate (22.6 mg, 0.061 mmol) in toluene (1 mL) at room temperature was added TsOH (5.8 mg, 0.030 mmol). The reaction mixture was heated at 80° C. for 1.5 h. The reaction mixture was diluted with EtOAc. The organic layer was washed consecutively with sat. aq. NaHCO3 (1×) and brine (1×), dried (Na2SO4), filtered and concentrated in vacuo to give methyl 6-(4-fluoro-5-isopropyl-2-methoxyphenyl)-3-methyl-1H-indene-5-carboxylate. LCMS calc.=377.2; found=376.9 (M+Na)+. 1H NMR (500 MHz, CDCl3): δ 7.85 (s, 1H); 7.41 (s, 1H); 7.14 (d, J=8.7 Hz, 1H); 6.63 (d, J=12.1 Hz, 1H); 6.30 (t, J=1.5 Hz, 1H); 3.72 (s, 3H); 3.72 (s, 3H); 3.42 (d, J=1.5 Hz, 2H); 3.29-3.21 (m, 1H); 2.25 (s, 3H); 1.31 (d, J=6.9 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-f697a7b0a3704cfd817909cacbbb8754
Source noteuspto-grants-2011_03