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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286089Generated: October 31, 2026

Hydrochloric Acid → HCID 54012237, compound

https://huagongshe.com/reaction/2286089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium NitriteHCID 23668193—
ReactantHCID 54310732HCID 54310732—
CatalystCuprous chlorideHCID 62652—
SolventWaterHCID 962—
ProductHCID 54012237HCID 54012237—

Reaction Steps

113.1 g of (6-amino-1,1,3,3-tetramethyl-5-indanyl) methyl ketone are suspended in 2260 ml of 20% hydrochloric acid and the suspension is cooled down to 0°-5° C. The cold mixture is treated dropwise within 10 minutes with a solution of 33.9 g of sodium nitrite in 115 ml of water and the resulting solution is stirred for 30 minutes. The cold solution is subsequently introduced dropwise over a period of 2 hours while stirring into a solution of 243.2 g of copper (I) chloride in 250 ml of water and 250 ml of concentrated hydrochloric acid, which is warmed to 40°-45° C. The mixture is then cooled down, introduced into ice-water and extracted three times with methylene chloride. The organic extract is washed with a sodium chloride solution, dried over sodium sulphate and freed from solvent under reduced pressure. The residue is purified by adsorption on silica gel using hexane/acetone (19:1) for the elution. The (6-chloro-1,1,3,3-tetramethyl-5-indanyl) methyl ketone obtained from the eluate melts at 69°-71° C. after recrystallisation from hexane/ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04326055
Source datasetuspto-grants-1982_04
ORD IDord-1be0c19507f64d108854e19283d9611a
Source noteuspto-grants-1982_04