HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510414Generated: November 4, 2026
o-Xylyl bromide → 2-(2-Methylbenzyl)-3-oxobutanenitrile
https://huagongshe.com/reaction/510414
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | o-Xylyl bromide | HCID 6992 | — |
| Reactant | HCID 178468205 | HCID 178468205 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | 2-(2-Methylbenzyl)-3-oxobutanenitrile | HCID 86724886 | 28% |
Reaction Steps
To a solution of (1-cyano-2-oxopropyl)sodium (525 mg, 5 mmol) in DMF (15 mL) was added 1-(bromomethyl)-2-methylbenzene (648 mg, 3.5 mmol) dropwise over a period of 15 min at 0° C. The mixture was stirred at 0° C. for 1 h and at room temperature for 2 h. Then this solution was diluted with saturated aq. ammonium chloride solution. This solution was extracted with ethyl acetate (30 mL×3). The combined organic layers were washed with water and brine, dried over Na2SO4, concentrated under reduced pressure. The residue was purified by a silica gel chromatography (petroleum ether/ethyl acetate=15/1) to give the titled product (181 mg, 28%) as a colorless oil; LC/MS: MS (ES+) m/e 188 (MH+); 1H NMR (300 MHz, CDCl3) δ ppm 2.35 (s, 3H), 2.38 (s, 3H), 3.06 (dd, J=9.6, 14.1 Hz, 1H), 3.28 (dd, J=5.4, 14.1 Hz, 1H), 3.60 (dd, J=5.4, 9.6 Hz, 1H), 7.18-7.22 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096605B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-7a9b70e32fc64191851f8450e9d60c9d |
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| Source note | uspto-grants-2015_08 |
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