HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397787Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 12493406, compound
https://huagongshe.com/reaction/2397787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Glycine Hydrochloride | HCID 22316 | — |
| Reactant | HCID 13341587 | HCID 13341587 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12493406 | HCID 12493406 | 57.9% |
Reaction Steps
To a solution of 4.5g of N,N'-dicyclohexylcarbodiimide in 100ml of dimethylformamide is added a solution of 2.2g of glycine hydrochloride in 2.2ml of water in a period of about 30 seconds under stirring and ice-cooling. Immediately a solution of 3.4g of 2-{[2-amino-5-bromo-α-(2-fluorophenyl)benzylidene]amino}ethanol in 10ml of tetrahydrofuran is added dropwise to the reaction mixture, and the mixture is stirred for further 3 hours at room temperature. After completion of the reaction, one liter of water is added to the reaction mixture which is extracted once with 100ml and four times with 50ml of benzene. The organic layer is washed with water, dried over anhydrous sodium sulfate, and the solvent is distilled off to give an oily substance, which is purified by chromatography of alumina column and then recrystallized from benzene-n-hexane (3:2 in volume) mixture yielding 2.3g of the desired product melting at 167°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04022832 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-f5b10d1ee51847449050d8eabcddf3b1 |
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| Source note | uspto-grants-1977_05 |
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