HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704718Generated: October 31, 2026
p-Bromoacetophenone → HCID 22758569, compound
https://huagongshe.com/reaction/1704718
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | N,N-Dimethylpropargylamine | HCID 81643 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Solvent | Ethylenediamine | HCID 3301 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22758569 | HCID 22758569 | — |
Reaction Steps
In 500 ml of ethylene diamine there is dissolved 13.88 g of lithium wire. After the disappearance of the blue color, the grey suspension obtained is dropwise treated, at 5° C., with 166.3 g of 3-dimethylamino-1-propyne. After 1 hour at room temperature, a solution of 50 g of p-bromoacetophenone in 250 ml of tetrahydrofuran is added. After 2 hours at room temperature, the mixture is poured onto ice and extracted with chloroform to give 62.9 g of crude, 2-(p-bromophenyl)-5-dimethylamino-3-pentyn-2-ol which is dissolved in 500 ml of acetone and treated with 18 ml of methyl iodide. After 18 hours at 5°, the solution is evaporated to dryness and the residue triturated with chloroform-ether to give 68 g of pure 2-(p-bromophenyl)-5-dimethylamino-3-pentyn-2-ol methiodide, mp 185°-190°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04127658 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-df37064fc8b645ff885dac7d5f175a1b |
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| Source note | uspto-grants-1978_11 |
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