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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969671Generated: October 30, 2026

Acetic Anhydride → 1-(4,4-dimethyl-7-nitro-3,4-dihydro-1H-isoquinolin-2-yl)ethanone

https://huagongshe.com/reaction/969671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4-Dimethyl-7-nitro-1,2,3,4-tetrahydroisoquinolineHCID 21959655—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(4,4-dimethyl-7-nitro-3,4-dihydro-1H-isoquinolin-2-yl)ethanoneHCID 21959565—

Reaction Steps

A mixture of 4-(dimethylamino)pyridine (0.125 g, 1.02 mmol), 4,4-dimethyl-7-nitro-1,2,3,4-tetrahydro-isoquinoline (0.21 g, 1.02 mmol), DIEA (0.53 mL, 3.06 mmol), and Ac2O (0.19 mL, 2.04 mmol) in 7 mL of CH2Cl2 was stirred at RT under N2 for two days. The volatiles were removed under vacuum. The residue was partitioned between EtOAc and brine, and the organic portion was dried with Na2SO4, filtered, and concentrated. The crude material was purified by flash column chromatography (2-3% MeOH in CH2Cl2), to yield the desired compound as a light yellowish solid. MS (ES+): 249.3 (M+H)+. Calc'd for C13H16N2O3-248.28.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307088B2
Source datasetuspto-grants-2007_12
ORD IDord-d1f9a01c9f3e470587ef7c783abd9c66
Source noteuspto-grants-2007_12