HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → tert-butyl N-[3-(tert-butoxycarbonylamino)-2-cyano-propyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | N,N'-di-Boc-2-methanesulfonyloxy-1,3-diaminopropane | HCID 14839452 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | tert-butyl N-[3-(tert-butoxycarbonylamino)-2-cyano-propyl]carbamate | HCID 375633 | 49.7% |
Reaction Steps
To a stirred solution of 2-[(tert-butoxycarbonyl)amino]-1-{[(tert-butoxycarbonyl)amino]methyl}ethyl methanesulfonate (10 g) in dimethyl sulfoxide (100 ml) was added sodium cyanide (2 g) at room temperature and the whole mixture was stirred overnight at room temperature. Water was added to the reaction mixture and the whole mixture was extracted with ethyl acetate. The extract was washed with water and brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residual oil was purified by column chromatography on silica gel (ethyl acetate:hexane=1:5) to give di-tert-butyl (2-cyano-1,3-propanediyl)biscarbamate (4.04 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07192943B2 |
| Source dataset | uspto-grants-2007_03 |
| ORD ID | ord-e61cafdd80254853a34ac8f52eff97d4 |
| Source note | uspto-grants-2007_03 |