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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702911Generated: November 1, 2026

32818-79-4 → HCID 5249961, compound

https://huagongshe.com/reaction/1702911

Reaction equation

Participants

RoleNameHCIDCharge
Reactant32818-79-4HCID 9576782—
Reactant2-Methylhexahydroisoquinoline-6,8(2H,7H)-dioneHCID 12855933—
ReactantHCID 12868345HCID 12868345—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
ProductHCID 5249961HCID 524996129%

Reaction Steps

1,2,3,4,4a,7-Hexahydro-6,8-dimethoxy-2-methylisoquinoline (0.56 g, 2.68 mmol) was heated to 90°-100° in 70% aqueous acetic acid (10 ml) to hydrolyze the bis(enolether) to the octahydro-2-methylisoquinolin-6,8-dione. To the hot solution was added zinc dust (0.6 g, 9.25 mmol) and 2-isonitroso-3-pentanone (0.7 g, 6.1 mmol). The mixture was refluxed for 3 hours, cooled and filtered to remove zinc and zinc acetate. The filtrate was concentrated to dryness on a rotary evaporator and the residue was dissolved in dichloromethane. To the solution was added ammonium hydroxide and the layers were separated. The organic layer was washed with brine and dried over anhydrous sodium sulfate and concentrated to give the crude product. Chromatography of the crude product on Alumina III afforded 3-ethyl-2,6-dimethyl-4,4a,5,6,7,8,8a,9-octahydro-1H-pyrrolo[2,3-g]isoquinolin-4-one as a white solid (0.19 g, 29% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04349678
Source datasetuspto-grants-1982_09
ORD IDord-c4769fdf0bc44ab89b09109d0e53b830
Source noteuspto-grants-1982_09