HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267820Generated: November 3, 2026
Bromoacetyl bromide → Acetamide, 2-bromo-N-methyl-N-2-propynyl-
https://huagongshe.com/reaction/267820
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | N-methylpropyn-2-ylamine | HCID 96160 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetamide, 2-bromo-N-methyl-N-2-propynyl- | HCID 10774018 | 85% |
Reaction Steps
A solution of 13.8 g (0.2 mol) of N-methylpropargylamine in 20 ml methylene chloride was added dropwise to a stirred and cooled (below 15°C.) solution of 40.2 g (0.2 mol) bromoacetyl bromide and 16 g (0.2 mol) sodium bicarbonate in 250 ml methylene chloride. The reaction mixture was allowed to warm to about 25°C. and stirred for 2 hours. The reaction mixture was then filtered and evaporated under reduced pressure to give an oily residue. The residue was diluted with 150 ml ether to form a two-phase mixture consisting of an ether phase and a dark oil. The ether phase was separated, dried over magnesium sulfate, and evaporated to give 32.3 g of N-methyl-N-propargyl-α-bromoacetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03944607 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-4e2ab9a786d7478fbf79ca559a0316c0 |
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| Source note | uspto-grants-1976_03 |
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