HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763787Generated: October 31, 2026
Benzene → N-(1,1-dimethylprop-2-ynyl)-N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-alpha-bromopropionamide
https://huagongshe.com/reaction/1763787
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Bromopropanoyl chloride | HCID 97980 | — |
| Reactant | HCID 20307430 | HCID 20307430 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(1,1-dimethylprop-2-ynyl)-N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-alpha-bromopropionamide | HCID 20307433 | — |
Reaction Steps
N-(1,1-Dimethylprop-2-ynyl)-N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)amine (10 grams), benzene (100 ml), water (100 ml) and sodium carbonate (8 grams) are charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The reaction mixture is cooled to a temperature of 5° to 10° C. and α-bromopropionyl chloride (7 grams) is added dropwise with stirring. After the addition is completed stirring is continued until the reaction mixture reaches room temperature. After this time the organic phase is separated from the aqueous phase and is washed with water. The washed solution is then dried over anhydrous magnesium sulfate, filtered and stripped of solvent under reduced pressure to yield the desired product N-(1,1-dimethylprop-2-ynyl)-N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-α-bromopropionamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04113464 |
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| Source dataset | uspto-grants-1978_09 |
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| ORD ID | ord-8fd29abf78944d6b87ed31d10ffd5cbf |
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| Source note | uspto-grants-1978_09 |
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