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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051615Generated: November 1, 2026

Ethyl chloroformate → HCID 20379307, compound

https://huagongshe.com/reaction/2051615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
Reactant3-Methyl-1,3-thiazolidin-2-imine hydroiodideHCID 2770507—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 20379307HCID 20379307—

Reaction Conditions

Temperature-5 °C

Reaction Steps

Ethyl chloroformate (0.25 ml.) at -5° C. was added to a solution of 350 mg. of t-butoxycarbonylaminoacetic acid and 0.4 ml. of triethylamine in 10 ml. of methylene chloride at -5° C. After stirring 5 minutes at -5° C. there was added a solution of 610 mg. of 2-imino-3-methylthiazolidine hydrogen iodide and 1.0 ml. of triethylamine in 10 ml. of methylene chloride also at -5° C. Stirring was continued at -5° C. for 15 minutes and one hour at room temperature. The reaction mixture was washed with 40 ml. of 20% (w/v) citric acid solution, sodium bicarbonate solution, and water, dried and concentrated to dryness. The residue was triturated with ether, petroleum ether and ether and finally collected to give pure N-(3-methylthiazolidin-2-ylidene)-t-butoxycarbonylaminoacetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04181661
Source datasetuspto-grants-1980_01
ORD IDord-282b45b8f3454126bcf896e4c191b799
Source noteuspto-grants-1980_01