HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → S-methyl-L-cysteine ethylamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | S-methyl-N-butyloxycarbonyl-L-cysteine ethylamide | HCID 57312465 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | S-methyl-L-cysteine ethylamide hydrochloride | HCID 86739336 | 94% |
Reaction Steps
To 60 ml of ice-cooled 16% solution of hydrogen chloride in ethyl acetate was added dropwise a solution of 3.93 g (15 mmole) of S-methyl-N-butyloxycarbonyl-L-cysteine ethylamide in 60 ml of ethyl acetate over 20 minutes. After stirring for 2 hours, the reaction mixture was concentrated in vacuo and the residual oil was treated with ethyl ether to give 2.8 g (94% yield) of S-methyl-L-cysteine ethylamide hydrochloride as powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440788 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-f4ecd067f5454a37ad5c0649b6210e4c |
| Source note | uspto-grants-1984_04 |