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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167662Generated: October 26, 2026

(E)-ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)acrylate → Ethyl 3-(3-((tert-butoxycarbonyl)amino)-4-chlorophenyl)propanoate

https://huagongshe.com/reaction/2167662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)acrylateHCID 67067541—
ReactantHCID 178418361HCID 178418361—
CatalystChlorotris(triphenylphosphine)rhodium(I)HCID 84599—
SolventEthanol ethylacetateHCID 21584252—
ProductEthyl 3-(3-((tert-butoxycarbonyl)amino)-4-chlorophenyl)propanoateHCID 67065553—

Reaction Steps

To a solution of (E)-ethyl 3-(3-(tert-butoxycarbonylamino)-4-chlorophenyl)acrylate (6-3) (1.0 equiv.) in ethyl acetate/ethanol (1:1, 0.3 M) was added Wilkinson's catalyst (0.10 equiv.). Hydrogen gas was introduced via a ballon, 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 (6-4) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045470B2
Source datasetuspto-grants-2015_06
ORD IDord-872f22a2b6d34d1c8ba6b71c8d536158
Source noteuspto-grants-2015_06