HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083838Generated: November 1, 2026
Dicyclohexylcarbodiimide → HCID 131711090, compound
https://huagongshe.com/reaction/2083838
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 12764079 | HCID 12764079 | — |
| Reactant | HCID 54560982 | HCID 54560982 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 131711090 | HCID 131711090 | — |
Reaction Steps
L-Tryptophyl-L-seryl-L-tyrosyl-D-phenylalanyl-L-leucine methyl ester (example 1, h), 1.6 g., is dissolved in 30 ml. of dimethylformamide and treated with 0.789 g., of Nα -p-methoxybenzyloxycarbonyl-O-benzyl-L-serine and cooled in an ice bath. 1-Hydroxybenzotriazole, 326 mg., and finally 500 mg., of dicyclohexylcarbodiimide are added and the reaction mixture stirred to room temperature overnight and for twenty-four additional hours. The reaction mixture is filtered and the solvent removed under reduced pressure. The residue is dissolved in 200 ml. of ethyl acetate and washed with 0.25 N hydrochloric acid, saturated sodium chloride solution, 5% sodium bicarbonate solution, and finally, saturated sodium chloride solution. The ethyl acetate solution is refrigerated for several days and a gelatinous precipitate separated. After triturating with ether for two hours, the above named product is separated and dried, 1.7 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04086219 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-eb14355f7bc949e190d6b0606657f50b |
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| Source note | uspto-grants-1978_04 |
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