HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1528873Generated: October 25, 2026
Ethyl diazoacetate → ethyl (1R,2R)-2-(4-bromophenyl)cyclopropanecarboxylate
https://huagongshe.com/reaction/1528873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | 4-Bromostyrene | HCID 16263 | — |
| Catalyst | Phenylhydrazine | HCID 7516 | — |
| Catalyst | Copper, bis(2,4-pentanedionato-O,O')-, (SP-4-1)- | HCID 5363992 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl (1R,2R)-2-(4-bromophenyl)cyclopropanecarboxylate | HCID 66578655 | — |
Reaction Steps
Copper(II) acetylacetonate (0.156 g, 0.6 mmol) was dissolved in CH2Cl2 (40 mL) then phenylhydrazine (3 drops, catalytic amount) was added. After 5 minutes, 4-bromostyrene (2.6 mL, 20 mmol) was added and the reaction was heated to 40° C. Ethyl diazoacetate (3.1 mL, 30 mmol) in CH2Cl2 (40 mL) was slowly added using a syringe pump. The reaction was stirred at 40° C. overnight then cooled and submitted to standard aqueous workup. The crude material was purified on silica gel (0-10% EtOAc in hexanes) two times to afford a separable mixture of two cyclopropyl isomers (cis- and trans-) and the less polar isomer was determined to be the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09090573B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-2b2737fdb7724d82a87c73e46ed606aa |
|---|
| Source note | uspto-grants-2015_07 |
|---|