HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051615Generated: November 1, 2026
Ethyl chloroformate → HCID 20379307, compound
https://huagongshe.com/reaction/2051615
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Reactant | 3-Methyl-1,3-thiazolidin-2-imine hydroiodide | HCID 2770507 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20379307 | HCID 20379307 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04181661 |
|---|
| Source dataset | uspto-grants-1980_01 |
|---|
| ORD ID | ord-282b45b8f3454126bcf896e4c191b799 |
|---|
| Source note | uspto-grants-1980_01 |
|---|