HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 23661730, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 57779803 | HCID 57779803 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 23661730 | HCID 23661730 | — |
Reaction Steps
A mixture of the crude product described above (1.01 g), N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.843 g, 4.39 mmol), 1-hydroxybenzotriazole (0.593 g, 4.39 mmol), diisopropylethylamine (1.90 mL, 11.0 mmol), the product from Step 3 (0.843 g, 2.42 mmol) and tetrahydrofuran (15 mL) was stirred for 18 hours at room temperature. The reaction was then diluted with H2O and extracted with ethyl acetate. The organic extracts were concentrated in vacuo and purified via flash chromatography on silica gel (0% to 50% ethyl acetate/hexanes linear gradient) to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888345B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-3773f60c3e95436fbae38d49aa48957e |
| Source note | uspto-grants-2011_02 |