HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489765Generated: October 30, 2026
1-Hydroxybenzotriazole → HCID 491693, compound
https://huagongshe.com/reaction/1489765
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide methyliodide | HCID 10236463 | — |
| Reactant | HCID 10707328 | HCID 10707328 | — |
| Reactant | HCID 67551723 | HCID 67551723 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 491693 | HCID 491693 | 65% |
Reaction Steps
To a mixture of 0.0643 g (0.24 mmol) of the acid from Step A, 0.0797 g (0.236 mmol) of the the amine from Step B, 0.032 g (0.24 mmol) of 1-hydroxybenzotriazole in 0.5 ml of anhydrous DMF was added 0.071 g (0.24 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide methiodide. After stirring overnight at room temperature the mixture was diluted to 30 ml with ethyl acetate and Washed successively with water, 5% aqueous sodium bicarbonate, 2% aqueous potassium bisulfate solution, and saturated sodium chloride solution and dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure and purification of the residue by column chromatography (silica gel, hexane/ethyl acetate 3:2) gave 0.091 g (65% yield) of the title compound, melting at 186°-189° C.: Rf (B)=0.19; Rf (C)=0.83; NMR (CDCl3) 1.0 (m, 12H, val and isopropyl CH3); 1.71 (s, 9H, t-butyl CH3); 2.3 (m, 1 H, val CH-β); 2.5-3.27 (m, 3H, butyl CH-3, CH2); 3.5 (m, 1 H, isopropyl CH); 4.31 (m, 2H, val CH-α, OH); 5.43 (broad s, 1 H, carbazate NH); 6.22 (broad d, 1H, butyl NH); 6.7-8.73 (m, 12H, aromatic, NH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05679688 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-224a4785269a4bccbc08c2d1c4d31e0e |
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| Source note | uspto-grants-1997_10 |
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