HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Sulfide → HCID 178523373, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | HCID 13175150 | HCID 13175150 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178523373 | HCID 178523373 | — |
Reaction Steps
4.4 g (40 mmol) of triethylamine and a solution of 2.8 ml (2 mmol) of isobutyl chloroformate in 20 ml of dry methylene chloride are added dropwise, in succession, to a solution, cooled to -10°, of 5.36 g (20 mmol) of 3-p-nitrobenzyloxycarbonylaminopropionic acid in 100 ml of dry methylene chloride. The reaction mixture is stirred for one hour at -18°, then for 11/2 hours a strong current of hydrogen sulphide is passed through and the mixture allowed to heat up to room temperature. After acidifying with 2N sulphuric acid, again in the cold, the organic phase is separated, dried and concentrated in vacuo. The 3-p-nitrobenzyloxycarbonylaminothiopropionic acid obtained can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518533 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-4dce4df2364d432ca039f7d0d7f0b6d6 |
| Source note | uspto-grants-1985_05 |