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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482368Generated: October 30, 2026

4-Methylmorpholine → HCID 22106655, compound

https://huagongshe.com/reaction/482368

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 0.5 N HCl. The organic layer was washed with 0.5 N HCl (3X), saturated aqueous NaHCO3 (3X), 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 numberUS05795900
Source datasetuspto-grants-1998_08
ORD IDord-9a117e4d311446a1bfea6a53ed7c559e
Source noteuspto-grants-1998_08