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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045371Generated: October 31, 2026

Water → HCID 67441782, compound

https://huagongshe.com/reaction/2045371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsobutyraldehydeHCID 6561—
ReactantYtterbium(3+) trifluoromethanesulfonate--water (1/3/1)HCID 45075687—
ReactantHCID 67442776HCID 67442776—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67441782HCID 6744178299.8%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a stirred mixture solution of 5-[(3-bromo-benzylidene)-amino]-2-chloro-benzoic acid methyl ester (39.8 g, 113.2 mmol) and ytterbium(III) triflate hydrate (10.5 g, 16.9 mmol) in dry tetrahydrofuran (100 mL) at 25° C. was added isobutyraldehyde (10.4 mL, 113.2 mmol) and water (2.1 mL, 113.2 mmol) dropwise. The reaction mixture was stirred at 25° C. for 16 h. Then the reaction mixture was concentrated in vacuo and the residue was extracted with ethyl acetate (2×200 mL), washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to afford 2-(3-bromo-phenyl)-6-chloro-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-5-carboxylic acid methyl ester (48 g, quant.) as a light yellow oil which was used for next step without further purification: LC/MS m/e calcd for C19H19BrClNO3 (M+H)+: 425.73, observed: 405.9 & 407.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586747B2
Source datasetuspto-grants-2013_11
ORD IDord-033c6bd1ae214c5598a5983b50a063f9
Source noteuspto-grants-2013_11