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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456869Generated: October 30, 2026

4-Methylmorpholine → HCID 22106655, compound

https://huagongshe.com/reaction/1456869

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantBenzeneacetic acid, 4-hydroxy-.alpha.-(4-hydroxyphenyl)-HCID 170289—
SolventHydrochloric AcidHCID 313—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22106655HCID 2210665590.5%

Reaction Steps

To a stirred solution in CH2Cl2 (0.5 mL), THF (20 mL), and pyridine (20 mL) of 2,2-bis(4-hydroxyphenyl)acetic acid (0.94 g, 3.85 mmol), prepared as in Example 31, was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (1.10 g, 5.76 mmol), glycine methyl ester hydrochloride (0.723 g, 5.76 mmol), and N-methylmorpholine (0.63 mL, 5,76 mmol) and the mixture was stirred overnight at room temperature. The reaction mixture was then diluted with ethyl acetate and aqueous 0.5N HCl. The organic layer was washed with 0.5N HCl (3×), saturated aqueous NaHCO3 (3×), and brine, dried over MgSO4, filtered, and concentrated in vacuo. The residue was dried to constant weight on high vacuum to give 1.05 g (87%) of 2,2-bis(4-hydroxyphenyl)acetic acid-N-carboxymethyl amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843968
Source datasetuspto-grants-1998_12
ORD IDord-67500e4c679d4cb694eee47d905fee17
Source noteuspto-grants-1998_12