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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582812Generated: November 2, 2026

Hydrochloric Acid → HCID 20726819, compound

https://huagongshe.com/reaction/1582812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 20726822HCID 20726822—
ReactantEthyl acetate hexaneHCID 21226206—
SolventEthanolHCID 702—
ProductHCID 20726819HCID 2072681976.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

Aqueous sodium hydroxide (1N, 1 ml) was added to ethyl 10-[(R)-7-hydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-benzo[1,4]-oxazine-4-yl]-2-(6,6,7,7,7-pentafluoroheptyl)decanoate (56.8 mg, 0.0902 mmol) in ethanol (1 ml) under a nitrogen stream, followed by stirring for 7 hours at 50° C. After cooling, the reaction mixture was acidified with 1N aqueous hydrochloric acid and extracted with ethyl acetate. The organic layer was washed sequentially with water and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/1, v/v) to give 10-[(R)-7-hydroxy-3-(4-hydroxyphenyl)-3,4-dihydro-2H-benzo[1,4]-oxazine-4-yl]-2-(6,6,7,7,7-pentafluoroheptyl)decanoic acid (41.4 mg, Yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06737417B2
Source datasetuspto-grants-2004_05
ORD IDord-34b0398eebb4457d8981ebcaaf385626
Source noteuspto-grants-2004_05