HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 15035854, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(tert-butoxycarbonyl)-2-aminoethanethiol | HCID 3017761 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15035854 | HCID 15035854 | 102.3% |
Reaction Steps
N-(t-butyloxycarbonyl)-aminoethanethiol (40 g, 225 mmole) from Example 2, and epichlorohydrin (35.4 g, 383 mmole) in 300 mL of ethanol were cooled to 0° C. and treated with potassium carbonate (35.4 g). The reaction was warmed to room temperature over 90 minutes and filtered through celite. The volatiles were removed under reduced pressure to give a clear oil (62.09 g, 100% yield) D.C.I.M.S. 270(M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075440 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-80c662197df04bcbaccf6213f4be7ac2 |
| Source note | uspto-grants-1991_12 |