HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1525613Generated: October 27, 2026
Dicyclohexylcarbodiimide → HCID 86640278, compound
https://huagongshe.com/reaction/1525613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Boc-L-Valine | HCID 83693 | — |
| Reactant | 1,2-Ethanediol, 1-nitrate | HCID 85254 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86640278 | HCID 86640278 | — |
Reaction Steps
To the reactor 2-hydroxyethyl nitrate (8 kg) was added, followed by dichloromethane (25 L). Then, boc-L-valine (12.5 kg) was added slowly under stirring, and the reaction mixture was cooled down to −10° C. Afterwards, DMAP (50 g) was added as the catalyst, and DCC (12.5 kg dissolved in 5 L of dichloromethame) was slowly added dropwise to the mixture under −10° C. The reaction was continued for another 5 hours at temperature between −10 and 0° under continuous stirring, while insoluble white solid was gradually formed. The reaction mixture was then warmed up slowly to room temperature, and the reaction was continued for another 12 hours at room temperature. At the end, the reaction mixture was filtered, and the filtrate was washed with water and dried to yield the crude nitrooxyethyl boc-valinate that was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085508B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-20d92f016b61477281263f3f7312419a |
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| Source note | uspto-grants-2015_07 |
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