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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269447Generated: October 29, 2026

Hydrochloric Acid → HCID 59832534, compound

https://huagongshe.com/reaction/269447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromineHCID 24408—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2,6-dimethyl-2,3-dihydroinden-1-oneHCID 11593477—
SolventDichloromethaneHCID 6344—
ProductHCID 59832534HCID 59832534—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 334 g (2.50 mol) of anhydrous AlCl3 (powder) in 400 ml of dry dichloromethane, a solution of 160 g (1.00 mol) of 2,6-dimethylindan-1-one in 200 ml of dichloromethane was added dropwise while vigorously stirring for 30 min at 0° C. This mixture was stirred for 1 h at ambient temperature, and then a solution of 51.6 ml (161 g, 1.01 mol) of bromine in 800 ml of dichloromethane was added while vigorously stirring for 2 h. The resulting mixture was stirred for 12 h and then poured on 700 cm3 of ice. The mixture was acidified by saturated HCl to pH 1, the organic layer was separated, and the aqueous layer was extracted with 3×350 ml of dichloromethane. The combined organic fractions were dried over K2CO3 and then evaporated to dryness. From the residue, 71.0 g of the starting indanone was distilled off in vacuum (bp 89-91 mm Hg), and the solid material left in the rectification flask was recrystallized from 600 ml of hot hexanes. Crystals that precipitated at room temperature were collected. The pure title product was then isolated by flash chromatography on Silica Gel 60 (40-63 um, d 50 mm, l 1200 mm, eluent: hexanes-dichloromethane, 10:1, vol.). Yield 44.0 g (18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446216B2
Source datasetuspto-grants-2008_11
ORD IDord-6414386a08eb44a1a60ecea3661e2dd7
Source noteuspto-grants-2008_11