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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854947Generated: October 30, 2026

Hydrochloric Acid → HCID 11380767, compound

https://huagongshe.com/reaction/854947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantLithium HydroxideHCID 3939—
ReactantHCID 69516975HCID 69516975—
SolventMethanol tetrahydrofuran waterHCID 21892291—
ProductHCID 11380767HCID 113807672,627.5%

Reaction Steps

Ethyl 6-chloro-8-methyl-2-(trifluoromethyl)-1,2-dihydroquinoline-3-carboxylate (4.5, 0.51 mmol) was suspended in methanol-tetrahydrofuran-water (50 mL, 7:2:1). Lithium hydroxide (1.70 g, 42.3 mmol) was added, and the mixture was gently heated to reflux for two hours. The reaction was cooled to room temperature and 1 N aqueous hydrochloric acid added until pH=1. The organic solvent was removed in vauco to afford a suspension of a crude yellow solid. Diethyl ether (200 mL) was added, and the solution was washed with water (2×200 mL), saturated ammonium sulfate (2×200 mL), dried over sodium sulfate and filtered. The filtrate was concentrated in vacuo to yield 6-chloro-8-methyl-2-(trifluoromethyl)-1,2-dihydroquinoline-3-carboxylic acid (3.8 g, 13.4 mmol) as a yellow solid (95% yield). (CDCl3, 300 MHz) 7.56 (s, 1H), 6.93 (s, 1H), 6.90 (s, 1H), 5.11 (q, 1H, J=7.2 Hz), 4.78 (bs, 1H), 2.08 (s, 3H). HRMS m/z 291.0286(M+, C12H9ClF3NO2, calcd 291.0274).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-1bfc582a7fc14da59fcb91d53738df35
Source noteuspto-grants-2007_08