HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594655Generated: October 27, 2026
1,1-Dibromoethane → Benzyl 3-phenylpropanoate
https://huagongshe.com/reaction/1594655
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Tri-o-tolylphosphine | HCID 80271 | — |
| Reactant | N-Boc-iodo-L-alanine benzyl ester | HCID 21968199 | — |
| Reactant | 1-(4-Iodophenyl)cyclopropane-1-carboxylate | HCID 86330814 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Benzyl 3-phenylpropanoate | HCID 562789 | 67.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06284768B1 |
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| Source dataset | uspto-grants-2001_09 |
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| ORD ID | ord-ac383dfc05024e9b8a6d92147fbc163f |
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| Source note | uspto-grants-2001_09 |
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