HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873782Generated: October 31, 2026
Diisopropylethylamine → HCID 149434098, compound
https://huagongshe.com/reaction/873782
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 110795-27-2 | HCID 13720922 | — |
| Reactant | Tert-butyl amino(imino)methylcarbamate | HCID 86691067 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 149434098 | HCID 149434098 | 100% |
Reaction Steps
(2E)-3-Mesitylacrylic acid (8.0 g; 42 mmol), diisopropylethylamine (27.2 g; 210 mmol), tert-butyl amino(imino)methylcarbamate (8.03 g; 50 mmol), and 1-hydroxybenzotriazole monohydrate (7.73 g; 50 mmol) were dissolved in N,N-dimethylformamide (170 mL), 2-(1H)-benzotriazol-1-yl-1,1,3,3-tetramethyluronium hexafluorophosphate (19.2 g; 50 mmol) was added thereto, and the mixture was stirred for 20 hours at room temperature. To the reaction solution, ethyl acetate (500 mL) was added, and the mixture was washed with 10% aqueous citric acid solution, brine, saturated aqueous sodium bicarbonate solution, and then brine. The organic layer was dried over anhydrous magnesium sulfate and then distilled under reduced pressure, to give 13.9 g of the title compound (yield 100%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975411B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-805090cec0cf4641ab350cfe8dfaf7f7 |
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| Source note | uspto-grants-2015_03 |
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