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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882371Generated: October 30, 2026

Pyridine → HCID 86696308, compound

https://huagongshe.com/reaction/882371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl glycinateHCID 409140—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Chloroethyl chloroformateHCID 521305—
ReactantBenzyl 2-aminoacetate hydrochlorideHCID 11701227—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86696308HCID 86696308—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Benzyl 2-aminoacetate was generated from a treatment of benzyl 2-aminoacetate hydrochloride (Aldrich) in methylene chloride with aqueous sodium bicarbonate solution followed by water wash. To a cooled solution of benzyl 2-aminoacetate (1.837 g, 11.1 mmol) and pyridine (1.1 g, 1.1 mL, 13.9 mmol) in methylene chloride (17 mL) at −78° C., was added slowly 1-chloroethyl chloroformate (Aldrich, 1.67 g, 11.7 mmol) over ˜10 min. The reaction mixture was allowed to stir at −78° C. for 3 h, giving a white precipitate. This cold reaction mixture was filtered to remove the solid and the filtrate was concentrated to dryness, giving the crude benzyl 2-((1-chloroethoxy)carbonylamino)acetate which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993614B2
Source datasetuspto-grants-2015_03
ORD IDord-f86db14a0f7547e3a6936716e2e6f02b
Source noteuspto-grants-2015_03