HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → N-(tert-butoxycarbonyl)-2-aminoethanethiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | tert-butyl N-(2-((2-aminoethyl)disulfanyl)ethyl)carbamate | HCID 22245556 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(tert-butoxycarbonyl)-2-aminoethanethiol | HCID 3017761 | 106.4% |
Reaction Steps
A solution of bis N-(t-butyloxycarbonyl)-cystamine (77.37 g, 0.220 mole) from Example 1, in 1 L of ethanol was treated with NaBH4 (32.5 g, 0.859 mmole). Vigorous gas evolution ensued and subsided in 40 minutes. The reaction was stirred for an additional half hour and was poured into 2.5 L of a cold dilute solution of citric acid (pH 6). The mixture was then extracted with 3×1 L of chloroform. The combined organic extracts were dried with MgSO4 and the solvents were removed under reduced pressure. The resulting residue was distilled (66°-73° C. 0.25 torr) to obtain the product (41.5 g, 53% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075440 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-7311b23c74dc40e28c313817a301885f |
| Source note | uspto-grants-1991_12 |