HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724344Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 131726110, compound
https://huagongshe.com/reaction/724344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-Bromopropionic acid | HCID 11729 | — |
| Reactant | Ether hydrochloride | HCID 10953452 | — |
| Reactant | HCID 131726111 | HCID 131726111 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 131726110 | HCID 131726110 | — |
Reaction Steps
Bromopropionic acid anhydride [formed by reacting bromopropionic acid (1.66 g, 10.86 mmol) with DCC (1.12 g, 5.43 mmol) in 20 ml anhydrous dichloromethane for 15 minutes at 25° C., and filtering off the solid that precipitated] was added to a solution of aminophenylarsineoxide (1 g, 5.43 mmol, synthesized according to published protocol) in 10 ml DMF, and allowed to stir overnight. The amino phenylarsineoxide was rendered soluble by adding to it 10.86 mmol HCl/ether followed by neutralization with triethylamine and filtering the away the solid that formed. The solution was quenched with 20 ml water, and filtered to remove solids. The filtrate was evaporated to an oil, and purified via flash chromatography. In later preparations, 3-bromopropionyl chloride was used instead of the anhydride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141655B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-13c03d408d394a80948533ff34f6f825 |
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| Source note | uspto-grants-2006_11 |
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