HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428921Generated: October 29, 2026
Ethyl diazoacetate → HCID 22141229, compound
https://huagongshe.com/reaction/428921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl diazoacetate | HCID 12192 | — |
| Reactant | HCID 69554694 | HCID 69554694 | — |
| Catalyst | Acetic acid, rhodium salt (4:2) | HCID 423677 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22141229 | HCID 22141229 | — |
Reaction Steps
To a solution of 3-[(E)-3-chloro-1-methyl-1-propenyl]benzonitrile (Preparation 34, 13.1 g, 69.6 mmol) in dichloromethane (20 md) was added rhodium (II) acetate dimer (0.46 g, 1.0 mmol). To the mixture was added dropwise at room temperature over 8 h (via a syringe pump) a solution of ethyl diazoacetate (14.6 ml, 0.14 mol) in dichloromethane (20 ml). The solvent was removed in vacuo and the crude residue was then partially purified by silica column chromatography eluting with dichloromethane:hexane (80:20). This material was then dissolved in dichloromethane (20 ml) containing rhodium (I) acetate dimer (0.46 g, 1.0 mmol). To this mixture was added dropwise a solution of ethyl diazoacetate (14.6 ml, 0.14 mol) in dichloromethane (20 ml) at room temperature over 8 h. The mixture was concentrated irn vacuo and the residue purified by silica column chromatography eluting with hexane:dichloromethane (80:20) and then hexane:diethyl ether (80:20) to give the title compound as a colourless oil which solidified on standing (5.82 g, 30%).
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-305574dd1b2641fe99bafc5b3903108b |
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| Source note | uspto-grants-2001_11 |
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