HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824486Generated: October 31, 2026
Potassium Hydroxide → HCID 12138719, compound
https://huagongshe.com/reaction/1824486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2,3-Dihydro-1,4-benzodioxin-6-carbaldehyde | HCID 248127 | — |
| Reactant | Pyrrolidine, 1-(isocyanoacetyl)- | HCID 6455476 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 12138719 | HCID 12138719 | 68.2% |
Reaction Steps
To a stirred and cooled (0° C.) solution of potassium hydroxide (2.70 g, 48.1 mmol) in methanol (30 ml) was added a mixture of 1,4-benzodioxan-6-carboxaldehyde (8.20 g, 50.0 mmol) and the product from Example 1 (6.30 g, 45.6 mmol). The solution was stirred overnight with continued cooling and then concentrated. The residue was partitioned between ethyl acetate and water. The organic layer was combined with additional ethyl acetate extracts, washed with aqueous sodium chloride and dried (magnesium sulfate). Concentration afforded crude product as a golden, glassy solid. Flash chromatography over silica (ethyl acetate) yielded 9.40 g (68%) of product as a colorless glassy solid. 1H NMR (CDCl3) δ 6.99 (s, 1H), 6.90–6.78 (m, 3H), 6.00 (d, J=7.3, 1H), 4.58, (d, J=7.3, 1H), 4.26 (s, 4H), 3.95–3.87 (m, 1H), 3.55–3.41 (m, 3H), 2.04–1.80 (m, 4H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041831B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-757d94dc4ee14ffd82bc11e9936d2697 |
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| Source note | uspto-grants-2006_05 |
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