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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389539Generated: October 30, 2026

Sulfuric Acid → HCID 59400175, compound

https://huagongshe.com/reaction/2389539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantHCID 59400150HCID 59400150—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
ProductHCID 59400175HCID 59400175—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of (S)—N—((S)-1-(4-fluorobenzyl)-1,2,3,4-tetrahydroquinolin-3-yl)-2-hydroxy-2-phenylacetamide (350 mg, 0.90 mmol) in absolute ethanol (20 mL) was added concentrated sulfuric acid (2 mL). The reaction mixture was stirred at 85° C. for 24 hours. The mixture was diluted with EtOAc (100 mL), 6 M NaOH aqueous solution (20 mL) and water (50 mL). The phases were separated and the aqueous phase was extracted with EtOAc (100 mL). The combined organic phases were washed with water (50 mL) and brine (50 mL), dried over anhydrous sodium sulfate and evaporated to dryness. The crude product was purified by flash chromatography using a gradient (0-10% MeOH in EtOAc). The desired product (S)-1-(4-fluorobenzyl)-1,2,3,4-tetrahydroquinolin-3-amine was obtained as yellow oil (169 mg, 73% yield). 1H NMR (DMSO-d6) 400 MHz δ 7.32-7.25 (m, 2H), 7.18-7.10 (m, 2H), 6.91-6.85 (m, 2H), 6.50-6.42 (m, 2H), 4.49 (d, J=16.8 Hz, 1H for AB system), 4.42 (d, J=16.8 Hz, 1H for AB system), 3.36-3.28 (m, 2H), 3.18-3.10 (m, 1H), 3.01 (dd, J=11.0, 8.6 Hz, 1H), 2.84 (dd, J=15.7, 2.7 Hz, 1H), 1.70 (br. s, 2H). LCMS m/e 258 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273754B2
Source datasetuspto-grants-2012_09
ORD IDord-c8bb9e0ccee84a15ae2e79ebf89ca416
Source noteuspto-grants-2012_09