Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 58764230 | HCID 58764230 | — |
| Product | HCID 86605373 | HCID 86605373 | 59% |
Reaction Steps
A solution of 5-(diethoxymethyl)-3-ethyl-1-methyl-1H-1,2,4-triazole from Step 3 (35.6 g, 0.167 mol) in 3.6 M HCl (150 mL) was heated (60° C.) for 10 h, then evaporated to dryness. The residual oil was washed with THF (3×100 mL), then treated with dry acetone (200 mL) causing crystallization. The product was filtered and dried, affording 18.8 g (59%) of the title product. Satisfactory C,H,N-analysis was obtained. The compound was observed by 1H NMR to be a 60:40 mixture of non-covalent (free aldehyde) and covalent hydrates, respectively. 1H NMR (400 MHz, DMSO-d6): δ 1.22 (m, overlap, 3H), 2.67 (q, J=7.8 Hz, 0.6×2H), 2.79 (q, J=7.8 Hz, 0.4×2H), 3.96 (s, 0.4×3H), 4.04 (s, 0.6×3H), 6.21 (s, 0.4×1H), 8.35 (br s, 3H), 9.87 (s, 0.6×1H). LC-MS (APCI) calcd for C6H9N3O: 139.07, found (M+H+): 140.1; (M+18+H+) 158.1 m/z.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07622605B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-c31e20d8f287440a8bf9e0f4ad406bb1 |
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| Source note | uspto-grants-2009_11 |
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