HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428909Generated: October 29, 2026
Ethyl diazoacetate → HCID 22141267, compound
https://huagongshe.com/reaction/428909
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | HCID 69554424 | HCID 69554424 | — |
| Catalyst | Acetic acid, rhodium salt (4:2) | HCID 423677 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22141267 | HCID 22141267 | 15.3% |
Reaction Steps
To a solution of 1-[(E)-3-chloro-1-ethyl-1-propenyl]-3-nitrobenzene (Preparation 15, 50 g, 0.22 mol) in dichloromethane (40 ml) was added rhodium (11) acetate dimer (2.0 g, 4.6 mmol). To the mixture was added dropwise at room temperature over 6 hours a solution of ethyl diazoacetate (50 ml, 54.25 g, 0.475 mol) in dichloromethane (50 ml), then the mixture stirred at room temperature for 16 hours. To the mixture was added dropwise at room temperature over 7 hours a solution of ethyl diazoacetate (20 ml, 21.70 g, 0.190 mol) in dichloromethane (20 ml), then the mixture was stirred at room temperature for 16 h. The mixture was concentrated in vacuo and the residue purified by silica column (1 kg) chromatography, eluting with 1:1 hexane/dichloromethane. Product-containing fractions were combined and concentrated in vacuo to give the title compound as a pale orange oil (10.5 g, 15%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313312B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-95f8a37af9aa4a21ae6bd7220266485a |
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| Source note | uspto-grants-2001_11 |
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