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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481781Generated: October 26, 2026

Water → 1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/481781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium borohydrideHCID 4311764—
Reactant1-Methyl-7-nitro-3,4-dihydroisoquinolineHCID 10932228—
SolventMethanolHCID 887—
Product1-Methyl-7-nitro-1,2,3,4-tetrahydroisoquinolineHCID 2158431182.5%

Reaction Steps

1.08 g of 1-methyl-7-nitro-3,4-dihydroisoquinoline was dissolved in 10 ml of methanol, and 0.43 g of sodium borohydride was added to the solution at 0° C. The solution was stirred overnight at room temperature, and water was added to the reaction mixture. The mixture was extracted with ethyl acetate, and after washing with saturated aqueous solution of sodium chloride, the solution was dried with anhydrous sodium sulfate. The desiccant was separated by filtration, and the filtrate was purified by silica gel column chromatography to obtain 0.90 g of 1-methyl-7-nitro-1,2,3,4-tetrahydroisoquinoline, which was an oily product (yield: 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789595
Source datasetuspto-grants-1998_08
ORD IDord-a27e714908bf4ba4b1cf51f6fb4b7765
Source noteuspto-grants-1998_08