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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352487Generated: October 26, 2026

Water → cis-2-Methyl-4-phenylamino-3,4-dihydro-2h-quinoline-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1352487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Methyl-4-phenylimino-3,4-dihydro-2H-quinoline-1-carboxylic Acid Benzyl EsterHCID 12093187—
SolventAcetic AcidHCID 176—
SolventCyclohexaneHCID 8078—
SolventSodium triacetoxyborohydrideHCID 5049666—
Productcis-2-Methyl-4-phenylamino-3,4-dihydro-2h-quinoline-1-carboxylic acid benzyl esterHCID 1209318846.6%

Reaction Steps

To a solution of 2-methyl-4-phenylimino-3,4-dihydro-2H-quinoline-1-carboxylic acid benzyl ester (16 g) in acetic acid (450 ml), sodium triacetoxyborohydride was added in small amounts (32.32 g), under stirring, at room temperature. The reaction mixture was then stirred at room temperature for one hour and poured on 1 liter of cold water under stirring. After precipitation, the mixture was filtered, dissolved in ethyl acetate and then, washed with water. The organic layer was separated and dried over sodium sulfate. The solvent was removed to give the crude compound (9g), recristallised in hot cyclohexane (40 ml), and then filtered at room temperature to give the desired compound (5.3 g, 46.6% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220760B2
Source datasetuspto-grants-2007_05
ORD IDord-1443954de1d64102a48a3d0065f448be
Source noteuspto-grants-2007_05