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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715846Generated: November 3, 2026

Isopropanol → Methyl 1,2,3,4-tetrahydroquinoline-7-carboxylate

https://huagongshe.com/reaction/1715846

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPerchloric AcidHCID 24247—
ReactantMethyl quinoline-7-carboxylateHCID 12554532—
CatalystHCID 178424882HCID 178424882—
SolventWaterHCID 962—
ProductMethyl 1,2,3,4-tetrahydroquinoline-7-carboxylateHCID 16244389—

Reaction Conditions

Temperature85 °C

Reaction Steps

1,2,3,4-Tetrahydro-quinoline-7-carboxylic acid methyl ester was obtained as follows: To a solution of his (pentamethyl-cyclopentadiene iridium dichloride) (32 mg, 0.02 equiv.) in a degassed mixture of isopropanol (9.5 ml) and water (0.5 ml) was added quinoline-7-carboxylic acid methyl ester (374 mg, 2.00 mmol) and perchloric acid (70% in water, 0.02 ml, 0.1 equiv.). The mixture was stirred at 85° C. for 17 hours, then the solvents were evaporated. The residue was purified by flash chromatography (heptane/ethyl acetate gradient), yielding 1,2,3,4-tetrahydro-quinoline-7-carboxylic acid methyl ester as a white solid, 305 mg (80%). MS (ISP): m/e=192.4 (M+H+); δII (300 MHz; CDCl3) 7.23 (1H, d), 7.13 (1H, s), 6.98 (1H, d), 3.86 (3H, s), 2.52 (2H, m), 3.32 (2H, t), 2.79 (2H, t), 1.94 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799933B2
Source datasetuspto-grants-2010_09
ORD IDord-177459e003c94dcf927a3bb83fae874d
Source noteuspto-grants-2010_09