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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486553Generated: October 29, 2026

Hydrochloric Acid → HCID 19095420, compound

https://huagongshe.com/reaction/486553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 19095320HCID 19095320—
SolventEthylene GlycolHCID 174—
ProductHCID 19095420HCID 1909542088.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

N-[2-(4,5-Dihydro-1H-benzo[g]indol-1-yl)ethyl]acetamide (5.0 g) was suspended in 60 ml of ethylene glycol and 25 ml of water under argon and treated with 5.0 g of powdered potassium hydroxide. The mixture was stirred at 120° C. for 18 hours, subsequently cooled and treated with 150 ml of 2N hydrochloric acid while cooling. The solution was washed with 200 ml of methylene chloride, the organic phase was extracted three times with 100 ml of 2N hydrochloric acid each time, the aqueous phases were combined and made strongly alkaline with 28% sodium hydroxide solution while cooling with ice. The aqueous solution was extracted once with 200 ml of methylene chloride and twice with 100 ml of methylene chloride each time, the organic phases were combined, dried with MgSO4 and freed from solvent. The residue, 4.0 g of brown oil, was chromatographed on 250 g of silica gel with methylene chloride/methanol mixtures (99:1 to 19:1) as the eluent. There were obtained 3.7 g (88%) of 1-(2-aminoethyl)-4,5-dihydro-1H-benzo[g]indole which was processed without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292732
Source datasetuspto-grants-1994_03
ORD IDord-d6bce2927b034c51855169fe35025835
Source noteuspto-grants-1994_03