HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974000Generated: October 31, 2026
Toluene → N-[4-dimethylamino-2-butynyl)-2-hydroxy-2-methyl-2-phenylacetamide
https://huagongshe.com/reaction/974000
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(4-dimethylamino-2-butynyl)benzoylformamide | HCID 57052728 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-dimethylamino-2-butynyl)-2-hydroxy-2-methyl-2-phenylacetamide | HCID 15023479 | — |
Reaction Steps
A solution of methylmagnesium bromide (10.23 m mol) in diethyl ether (3.5 ml) and tetrahydrofuran (5 ml) were added to a solution of N-(4-dimethylamino-2-butynyl)-benzoylformamide (0.50 g) in toluene (8 ml) at room temperature. After being heated at 70° C. for 1.5 hours, the mixture was treated with 1N aqueous solution of sodium hydroxide and extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and evaporated in vacuo. The residue was purified by column chromatography on silica gel with a mixture of chloroform and methanol (15:1) as an eluent to give N-[4-dimethylamino-2-butynyl)-2-hydroxy-2-methyl-2-phenyl-acetamide (0.21 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066680 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-85164694e30145108a31e54a27703f1a |
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| Source note | uspto-grants-1991_11 |
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