HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023851Generated: November 4, 2026
Sodium borohydride → HCID 178521391, compound
https://huagongshe.com/reaction/1023851
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178521390 | HCID 178521390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178521391 | HCID 178521391 | 84% |
Reaction Steps
To a solution of 2-(2-(1H-imidazol-4-yl)phenoxy)-1-(3-bromophenyl)ethanone (0.025 g, 0.0699 mmol) in MeOH (2 mL) at room temperature, was added NaBH4 (0.349 mmol) and the resulting suspension was stirred for 1.5 h. The reaction was quenched by adding 1N HCl followed by basification with saturated Na2CO3 solution. The product was extracted with EtOAc (3×10 mL), organic extract was dried (Na2SO4) and concentrated under reduced pressure to afford yellow solid. The crude was subjected to column chromatography to afford the final product. Yield 84%. 1H NMR: 3.48 (s, 1H), 4.08 (t, 1H, J=9.39 Hz), 4.40 (dd, 1H, J=3.06, 6.69 Hz), 5.18 (dd, 1H, J=3.48, 5.85 Hz), 6.97 (d, 1H, J=7.59 Hz), 7.04 (d, 1H, J=7.59 Hz), 7.19-7.28 (m, 3H), 7.40 (d, 1H, J=8.73 Hz), 7.46 (d, 1H, J=7.80 Hz), 7.55-7.59 (m, 2H), 7.66 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722720B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-b7642fb185eb41d9a300ccd1a42524bc |
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| Source note | uspto-grants-2014_05 |
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