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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585081Generated: October 27, 2026

Nitroethane → Ethyl 2-(3,5-dihydroxyphenyl)-8,9-dimethoxy-3-methyl-5,6-dihydro-pyrrolo[2,1-a]-isoquinoline-1-carboxylate

https://huagongshe.com/reaction/585081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitroethaneHCID 6587—
ReactantPiperidineHCID 8082—
Reactant3,5-DihydroxybenzaldehydeHCID 94365—
Reactantethyl 2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)acetateHCID 70037591—
SolventIsopropanolHCID 3776—
SolventIsopropanol ethanolHCID 22179027—
ProductEthyl 2-(3,5-dihydroxyphenyl)-8,9-dimethoxy-3-methyl-5,6-dihydro-pyrrolo[2,1-a]-isoquinoline-1-carboxylateHCID 1011304812.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 500 mg (1.8 mmol) of ethyl (6,7-dimethoxy-3,4-dihydro-1(2H)-isoquinolinylidene)-ethanoate (Example III.1), 499 mg (3.61 mmol) of 3,5-dihydroxybenzaldehyde, 281 mg (3.61 mmol) of nitroethane and 61.4 mg (0.72 mmol) of piperidine in 10 mL of an ethanol/isopropanol 1:1 mixture was stirred at 80° C. overnight. 40 mL of isopropanol were added, the mixture was cooled to 0° C., and the resulting precipitate was filtered off. The solid was washed with ethanol and dried in vacuo to give the title compound as a white solid which was readily recrystallized from ethyl acetate to furnish white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930114B2
Source datasetuspto-grants-2005_08
ORD IDord-aa8fd636a9504701a856c152ff2eaebb
Source noteuspto-grants-2005_08