HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → Thioformamido-diethylphosphonoacetic acid tert.-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | HCID 57315705 | HCID 57315705 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Thioformamido-diethylphosphonoacetic acid tert.-butyl ester | HCID 86735044 | — |
Reaction Steps
Dry hydrogen sulphide gas is passed for 10 minutes into a solution, cooled to 0° C., of 277 mg (1 mmol) of diethylphosphono-isocyanoacetic acid tert.-butyl ester in 5 ml of dry tetrahydrofurane (filtered through aluminum oxide). After adding a few crystals of copper-II acetylacetonate, the reaction vessel is closed and left to stand overnight at room temperature. The reaction mixture is filtered and the filtrate is evaporated in vacuo. The residue is chromatographed on silica gel thick layer plates with toluene/ethyl acetate, 1:1, and gives thioformamido-diethylphosphonoacetic acid tert.-butyl ester in the form of a colorless oil: IR spectrum (in methylene chloride): characteristic bands at 3:13; 3.35; 5.75; 7.01; 8.10; 8.70 and 9.75μ.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04045520 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-ea91dd2c757d462f88140cae540178c9 |
| Source note | uspto-grants-1977_08 |