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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180577Generated: October 26, 2026

Dimethyl Sulfate → 5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/1180577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
Reactant5-Bromo-8-nitroisoquinolineHCID 816983—
ReactantSodium borohydrideHCID 4311764—
SolventAcetic AcidHCID 176—
Product5-Bromo-2-methyl-8-nitro-1,2,3,4-tetrahydroisoquinolineHCID 10016010—

Reaction Conditions

Temperature100 °C

Reaction Steps

5-Bromo-8-nitroisoquinoline (216.9 g, 0.86 mol) was added in portions during 10 min to a solution of dimethylsulphate (750 ml). Some heat was developed. The mixture was heated at 100° C. for 10 minutes. 5-Bromo-2-methyl-8-nitroquinolinium methyl sulphate precipitated. The mixture was cooled on ice and diethyl ether (1 l) was added. The crude mixture was filtered and crystals were isolated. The salt was solved in acetic acid (1.5 l). To the ice-cooled mixture was added: sodium borohydride (47 g, 1.24 mol) over 4 hours. The temperature was kept below 30° C. The crude mixture was evaporated and sodium hydroxide (2 l, 1 M) was added. The crystals were filtered. Yield 205.2 g (88%). Mp 85-87° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07282511B2
Source datasetuspto-grants-2007_10
ORD IDord-6a679fbecc35413abec6e948c4bcf4a6
Source noteuspto-grants-2007_10