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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406504Generated: October 30, 2026

2,6-Lutidine → HCID 86700769, compound

https://huagongshe.com/reaction/2406504

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant4-Bromo-5-hydroxy-2,3-dihydro-1H-inden-1-oneHCID 68866790—
SolventDichloromethaneHCID 6344—
ProductHCID 86700769HCID 86700769—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoromethanesulfonic anhydride (4.0 mL) is added dropwise to a solution of 4-bromo-5-hydroxy-indan-1-one (5.0 g) and 2,6-dimethylpyridine (5.1 mL) in dichloromethane (50 mL) cooled to 0° C. The cooling bath is removed and the mixture is stirred for 2 h at room temperature. The solution is partitioned between saturated aqueous NH4Cl solution and dichloromethane. The organic phase is separated, washed with brine, dried (MgSO4), and concentrated. The residue is chromatographed on silica gel (cyclohexane/ethyl acetate 99:1→50:50) to give the title compound. LC (method 2): tR=1.08 min; Mass spectrum (ESI+): m/z=359/361 (Br) [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809376B2
Source datasetuspto-grants-2014_08
ORD IDord-d7bff5d43bf64878b974949346eeaae3
Source noteuspto-grants-2014_08