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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911135Generated: November 3, 2026

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

https://huagongshe.com/reaction/1911135

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 numberUS08604017B2
Source datasetuspto-grants-2013_12
ORD IDord-3ab21e2866dc40799f5856e31a1d883a
Source noteuspto-grants-2013_12