HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → (-)-4'-{2-[4-(4-Nitrobenzyl)-2,5-dioxoimidazolidinyl]ethyl}acetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | N-[4-(2-hydroxyethyl)phenyl]acetamide | HCID 3295905 | — |
| Reactant | Diethyl azodicarboxylate | HCID 5462977 | — |
| Reactant | 5-[(4-Nitrophenyl)methyl]imidazolidine-2,4-dione | HCID 10466579 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | (-)-4'-{2-[4-(4-Nitrobenzyl)-2,5-dioxoimidazolidinyl]ethyl}acetanilide | HCID 19752550 | 71.8% |
Reaction Steps
A solution of diethylazodicarboxylate (7.8 g) in DME (40 ml) was added dropwise under N2 to a stirred mixture of the product from step (a) (10.5 g), the product from step (c) (8.0 g) and triphenylphosphine (11.7 g) in DME (400 ml). When addition was complete, the mixture was stirred at room temperature for 17 hours, then evaporated in vacuo and the residue crystallised from ethanol/ether (1:4 v/v) to give the desired product as a pale yellow solid (12.7 g), [α]D25 -97.8° (c=0.50, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225431 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-7b7f32cdc2c7499fab5cf10b83476cad |
| Source note | uspto-grants-1993_07 |