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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831723Generated: November 1, 2026

Acetic Anhydride → HCID 22052544, compound

https://huagongshe.com/reaction/1831723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178442067HCID 178442067—
ProductHCID 22052544HCID 2205254474%

Reaction Steps

100 Milligrams of 4-hydroxy-2,3-dimethyl-6-n-pentyl-quinoline (Compound No. 97) was stirred in 2 ml of acetic anhydride at 120° C. for 4 hours. After the solvent was evaporated, 20 ml of ethyl acetate was added and the reaction mixture was washed with an aqueous saturated sodium hydrogencarbonate solution and a saturated brine and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, the resultant crude product was purified by column chromatography on silica gel (WAKOGEL® C-100) eluting with n-hexane/ethyl acetate (5:1) to obtain 87.4 mg of 4-acetoxy-2,3-dimethyl-6-n-pentyl-quinoline (yield 74%). Its NMR spectral data are shown in the following Table 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067668B2
Source datasetuspto-grants-2006_06
ORD IDord-c07009cfa0684eb897286e55174d5514
Source noteuspto-grants-2006_06