HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026787Generated: October 31, 2026
Dicyclohexylcarbodiimide → HCID 53245019, compound
https://huagongshe.com/reaction/1026787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Perbenzoic acid | HCID 523077 | — |
| Reactant | HCID 67236283 | HCID 67236283 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Ethyl ether methylene chloride | HCID 21881112 | — |
| Product | HCID 53245019 | HCID 53245019 | 63.1% |
Reaction Steps
5 g (24 mmol) of 2-acetoxymethoxy-benzoic acid (prepared as described in example 1-2) and 3.3 g (24 mmol) of benzenecarboperoxoic acid are dissolved in 150 mL of diethyl ether/dichloromethane mixture, 6/4. The solution is cooled to 0° C., then 4.9 g (24 mmol) of N,N′-dicyclohexylcarbodiimide dissolved in 85 ml of diethyl ether is added dropwise. After stirring for 3 hours at 0° C., the reaction mixture is filtered and then concentrated. The residue is precipitated in diethyl ether and the filtrate is concentrated under reduced pressure. 5 g of (2-acetoxymethoxy-benzoyl)benzoyl peroxide is obtained in the form of white solid at a yield of 63%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729312B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-21377ae6b175424a90da9223e0fb8004 |
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| Source note | uspto-grants-2014_05 |
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