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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401650Generated: October 29, 2026

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

https://huagongshe.com/reaction/401650

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 numberUS08741887B2
Source datasetuspto-grants-2014_06
ORD IDord-23d2c8b03159411bbe5062b878a78be3
Source noteuspto-grants-2014_06