HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → L-Cysteine, N-acetyl-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | N-Acetyl-L-Cysteine | HCID 12035 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | L-Cysteine, N-acetyl-, methyl ester | HCID 6542158 | — |
Reaction Steps
N-Acetyl-L-cysteine (5 g, 30.6 mM) was treated with excess diazomethane (generated from N-nitrosomethyl urea) in ether for 6 hr at RT. Unreacted starting material was removed by filtration and the resulting yellow filtrate was allowed to stand overnight. The solvent was removed in vacuo and the residue crystallized from Et2O/Pet. ether to give pure N-acetyl-L-cysteine methyl ester (650 mg); mp 73°-76° C. compared to a literature mp of 81°-82° C. in the Journal of Organic Chemistry, Vol. 35, p. 3542 (1970) and 79°-80° C. in the Canadian Journal of Chemistry, Vol. 44, p. 2517 (1966).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04665092 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-159c22d30ab1487faf381c7ce26d6610 |
| Source note | uspto-grants-1987_05 |