HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755455Generated: November 2, 2026
2-Bromopropanedial → HCID 86700106, compound
https://huagongshe.com/reaction/1755455
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopropanedial | HCID 74945 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | HCID 86700105 | HCID 86700105 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86700106 | HCID 86700106 | 62.6% |
Reaction Steps
To a solution of material from Example 48 (5.25 g, 15.75 mmol) in a mixture of THF (178 mL) and acetic acid (29.6 mL), is added sequentially sodium acetate (1.55 g, 18.91 mmol) and 2-bromomalonaldehyde (2.75 g, 17.33 mmol) and the reaction is stirred at room temp. for 2 h. The solvent is removed in vacuo and the residue is partitioned between water (25 mL) and CH2Cl2 (40 mL). The aqueous phase is extracted with CH2Cl2 (2×20 mL), neutralized to pH 8 with solid sodium bicarbonate and extracted again with CH2Cl2 (3×25 mL). The organic layers are combined, washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The residue is purified by BIOTAGE® Silica gel chromatography on a 160 g Thompson Single Step silica cartridge using a linear gradient from 60% Hexanes/Ethyl Acetate to 50% Hexanes/Ethyl Acetate over 5 column volumes to give 3.8 g (62.6%) of the title compound as a yellow foam. LC/MS (Condition A): ret. T=3.52 min, (M+Na) 408.15. 1H NMR (400 MHz, DMSO-d6) δ ppm 9.64 (1 H, s), 8.94 (1 H, br. s.), 8.06 (1 H, s), 7.28 (1 H, d, J=7.78 Hz), 3.79-3.96 (1 H, m), 1.92-2.05 (1 H, m), 1.75-1.92 (1 H, m), 1.43 (3 H, br. s.), 1.40 (18 H, d, J=1.76 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169295B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-53a2e6d399ef44fdbd1702eabf0e05b3 |
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| Source note | uspto-grants-2015_10 |
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