HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbonodithioic acid, O-ethyl ester → (-)-alpha-Amino-3-[[(ethoxythioxomethyl)thio]methyl]-4-hydroxybenzeneacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbonodithioic acid, O-ethyl ester | HCID 1248527 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | (-)-alpha-Amino-3-(chloromethyl)-4-hydroxybenzeneacetic acid hydrochloride | HCID 70578051 | — |
| Solvent | Water | HCID 962 | — |
| Product | (-)-alpha-Amino-3-[[(ethoxythioxomethyl)thio]methyl]-4-hydroxybenzeneacetic acid | HCID 23329752 | 58.3% |
Reaction Steps
To a solution of (-)-α-amino-3-(chloromethyl)-4-hydroxybenzeneacetic acid hydrochloride (1 g, 0.004 mole) in 20 ml of water is added carbonodithioic acid, O-ethyl ester, potassium salt (1.26 g, 0.08 mole). Within a few minutes a precipitate begins to form. The mixture is stirred at room temperature for 3 hours. The solid precipitate is filtered, washed with water and dried to give 58.3% of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229363 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-eb83b1fcb5e242a9b96094a64d08fdac |
| Source note | uspto-grants-1980_10 |