HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 14696294, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,2'-Dipyridyl disulfide | HCID 65093 | — |
| Reactant | Cumylamine | HCID 68509 | — |
| Reactant | L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)- | HCID 90234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14696294 | HCID 14696294 | — |
Reaction Steps
11.0 g of powdery N-(t-butoxycarbonyl)-O-benzyl-L-serine were added to 200 ml of a methylene chloride solution containing 5.0 g of α,α-dimethylbenzylamine and 10.0 g of triphenylphosphine. 20 ml of a methylene chloride solution containing 8.2 g of 2,2'-dipyridyl disulfide were then added dropwise. The mixture was then stirred for 1 hour at room temperature, after which the solvent was distilled off under reduced pressure and the residue was subjected to silica gel column chromatography. The title compound was obtained as an oil from the fraction eluted with a 2:1 by volume mixture of ethyl acetate and hexane. Yield 9.2 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04904680 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-3553447fded0426b91ae717cbfc8f022 |
| Source note | uspto-grants-1990_02 |