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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950752Generated: October 29, 2026

Ethyl Acetate → HCID 59615955, compound

https://huagongshe.com/reaction/1950752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 131730352HCID 131730352—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59615955HCID 5961595585.9%

Reaction Steps

To a cooled (0° C.) solution of 6-[3,5-Bis-(tert-butyl-dimethyl-silyloxymethyl)-phenyl]-hex-5-ynoic acid methyl ester (140 mg) in anhydrous tetrahydrofurane (0.3 mL) was slightly added a solution of tetrabutylammonium fluoride 1 M in THF (716 μL). After 75 min at rt, ethyl acetate (20 mL) was added and the organic phase was washed three times with water (5 mL) and once with a saturated aqueous solution of sodium chloride (5 mL), dried over sodium sulfate and concentrated in vacuo to a residue. The residue was purified by silica gel chromatography (Merck SuperVarioFlash 15 g column, Si60 15-40 μm), using gradient elution with a mixture of heptane (A)/ethyl acetate (B), (gradient: 50% A: 50% B down to 10% A: 90% B) to give 6-(3,5-Bis-hydroxymethyl-phenyl)-hex-5-ynoic acid methyl ester (64.3 mg) as a pale yellow oil. LC/MS (Method A3): ES: m/z 263 (M+H)+; RT=0.62 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404678B2
Source datasetuspto-grants-2013_03
ORD IDord-15a90120046f4831862f992be428bf9a
Source noteuspto-grants-2013_03