HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420482Generated: October 26, 2026
Isopropylethanediol → Dimethyl 1-(2-isopropoxyethyl)-4-nitro-1H-pyrazole-3,5-dicarboxylate
https://huagongshe.com/reaction/420482
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropylethanediol | HCID 7996 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | dimethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate | HCID 1421248 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Dimethyl 1-(2-isopropoxyethyl)-4-nitro-1H-pyrazole-3,5-dicarboxylate | HCID 57799200 | — |
Reaction Steps
Dimethyl 4-nitro-1H-pyrazole-3,5-dicarboxylate (11.4 g, 50 mmol) was dissolved in tetrahydrofuran (200 mL) and the solution treated with triphenylphosphine (14.4 g, 55 mmol) and 2-isopropoxyethanol (6.36 mL, 55 mmol). The mixture was cooled on an ice bath to 0° C. and diisopropyl azodicarboxylate (10.8 mL, 55 mmol) added dropwise over 10 minutes, keeping the temperature between 20° C. and 30° C. The reaction mixture was then stirred at room temperature for 30 minutes. The reaction mixture was concentrated in vacuo and the crude product azeotroped with dichloromethane to yield the title product. 1H NMR (CDCl3, 400 MHz) δ: 1.02 (d, 6H), 3.45 (m, 1H), 3.72 (t, 2H), 3.90 (s, 3H), 3.94 (s, 3H), 4.74 (t, 2H). MS ES+ m/z 216 [MH]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097621B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-1be403a3cf1a42468cf95cd10f3297c1 |
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| Source note | uspto-grants-2012_01 |
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