HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373293Generated: October 29, 2026
Dicyclohexylcarbodiimide → HCID 86746314, compound
https://huagongshe.com/reaction/373293
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | HCID 19780620 | HCID 19780620 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86746314 | HCID 86746314 | — |
Reaction Steps
To a solution of 1.0 g of (2-benzoylthioacetyl)glycylglycylglycine (2.72 mmol) in 10 mL of dimethylforamide was added 0.56 g of dicyclohexylcarbodiimide (2.72 mmol) and 0.31 g of N-hydroxysuccinimide (2.72 mmol). The solution was stirred at room temperature for 24 hours. The resultant white solid was filtered off. The solvent was removed from the filtrate by rotary evaporator (vacuum pump, 35.) to give the product as a yellow semisolid. This solid was dried under vacuum overnight. The product was then recrystallized from 100 mL of hot 2-propanol to give 0.27 g of a white powder after filtration and drying under vacuum (21%). NMR (DMSO-d6)δ 2.81 (s, 4H), 3.79 (m, integral obscured by water), 3.89 (s, integral obscured by water), 4.28 (d, 2H), 7.58 (d, 2H), 7.71 (t, 1H), 7.93 (d,2H), 8.29 (br t, 1H), 8.54 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05162505 |
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| Source dataset | uspto-grants-1992_11 |
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| ORD ID | ord-363282513e0b44a7bee005e9856048b6 |
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| Source note | uspto-grants-1992_11 |
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