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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1950754Generated: October 29, 2026

Ethyl Acetate → HCID 59615978, compound

https://huagongshe.com/reaction/1950754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59615929HCID 59615929—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 59615978HCID 59615978—

Reaction Steps

To a cooled (0° C.) solution of N-[2-(3,5-Bis-hydroxymethyl-phenoxy)-ethyl]-N-methyl-succinamic acid (225 mg) in methanol (1 mL), was added (trimethylsilyl)diazomethane 2M in hexanes (840 μL) until persistence of the yellow colour. After 40 min, ethyl acetate (5 mL) and acetic acid (50 μL) were added, then, one minute later, a saturated aqueous solution of sodium hydrogen carbonate until pH=7. The aqueous phase was extracted with ethyl acetate. The combined organic layers were washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo to a residue. The residue was purified by silica gel chromatography (Merck SuperVarioFlash 25 g column, Si60 15-40 μm), using gradient elution with a mixture of DCM (A)/MeOH (B), (gradient: 98% A: 2% B down to 90% A: 10% B) to give N-[2-(3,5-Bis-hydroxymethyl-phenoxy)-ethyl]-N-methyl-succinamic acid methyl ester (103 mg). LC/MS (Method A3): ES: m/z 348 (M+Na)+; m/z 326 (M+H)+ m/z 308 (M−H2O+H)+; RT=0.43 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404678B2
Source datasetuspto-grants-2013_03
ORD IDord-29d80cea1cc04c69bbd7e3f5673f0566
Source noteuspto-grants-2013_03