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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594655Generated: October 27, 2026

1,1-Dibromoethane → Benzyl 3-phenylpropanoate

https://huagongshe.com/reaction/1594655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DibromoethaneHCID 11201—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantN-Boc-iodo-L-alanine benzyl esterHCID 21968199—
Reactant1-(4-Iodophenyl)cyclopropane-1-carboxylateHCID 86330814—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductBenzyl 3-phenylpropanoateHCID 56278967.1%

Reaction Conditions

Temperature55 °C

Reaction Steps

A suspension of zinc (0.874 g) in THF with dibromoethane (0.02 mL) was sonicated at 40° C. for 40 minutes under argon. N-Boc-iodo-L-alanine benzyl ester (4.20 g, 10.4 mmol) and dimethylacetamide (5 mL) were added, and the mixture was heated at 55° C. for 1 hour. tbutyl 1-(4-iodophenyl)cyclopropane-1-carboxylate (3.26 g, 9.48 mmol) in dimethylacetamide (10 mL) was added followed by tris(dibenzylideneacetone)dipalladium(0) (0.33 g) and tri-o-tolylphosphine (0.398 g). Heating was continued under argon for 16 hours. The mixture was diluted with ethyl acetate, washed with water, dried, filtered and evaporated. Chromatography of the residue over silica gel (methylene chloride/hexane 1/3 to methylene chloride/ethyl acetate 95/5) gave 2-(S)-tbutoxycarbonylamino-3-[4′-1″-tbutoxycarbonyl)cyclopropyl]benzenepropanoic acid benzyl ester (3.15 g, 6.36 mmol, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06284768B1
Source datasetuspto-grants-2001_09
ORD IDord-ac383dfc05024e9b8a6d92147fbc163f
Source noteuspto-grants-2001_09