HuagongsheHuagongshe Chemistry Print Report · For research reference only
(E)-ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)acrylate → Ethyl 3-(3-((tert-butoxycarbonyl)amino)-4-chlorophenyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (E)-ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)acrylate | HCID 67067541 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Chlorotris(triphenylphosphine)rhodium(I) | HCID 84599 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | Ethyl 3-(3-((tert-butoxycarbonyl)amino)-4-chlorophenyl)propanoate | HCID 67065553 | — |
Reaction Steps
To a solution of (E)-ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)acrylate (3) (1.0 equiv.) in ethyl acetate/ethanol (1:1, 0.3M) was added Wilkinson's catalyst (0.10 equiv.). Hydrogen gas was introduced via a balloon, and the reaction was stirred at room temperature for 24 hours. The mixture was filtered through a pad of celite, washing with dichloromethane. The filtrate was concentrated in vacuo and purified by Combiflash using 0-10% ethyl acetate in hexane to give ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)propanoate (4) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09320748B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-335b78c30bf747328bb40846151092b0 |
| Source note | uspto-grants-2016_04 |