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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023071Generated: October 30, 2026

Lithium Hydroxide → 1-Acetyl-6-bromo-1,2,3,4-tetrahydroquinoline-2-carboxylic acid

https://huagongshe.com/reaction/1023071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
Reactant1-Acetyl-6-bromo-1,2,3,4-tetrahydro-quinoline-2-carboxylic acid methyl esterHCID 59625992—
SolventMethanol tetrahydrofuran waterHCID 21892291—
Product1-Acetyl-6-bromo-1,2,3,4-tetrahydroquinoline-2-carboxylic acidHCID 59625947—

Reaction Steps

To a solution of compound 25b (116 mg, 0.37 mmol) in THF/MeOH/H2O (2/2/2 mL) was added LiOH (62 mg, 1.48 mmol). The reaction mixture was stirred at room temperature for 3 h. The resultant mixture was concentrated under reduced pressure, partitioned between CH2Cl2 and H2O, and the aqueous phase was brought to pH 5 by the addition of 2N HCl (aq). The organic phase was dried over Na2SO4, filtered, and concentrated under reduced pressure to give the crude compound 25c, which was used in the next step without further purification. LC/MS m/z 298.0 (M+H+), 300.0 (M+2H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722658B2
Source datasetuspto-grants-2014_05
ORD IDord-0b6998c9bd08449b9c1c6133f2032c2d
Source noteuspto-grants-2014_05