HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722700Generated: October 31, 2026
p-Aminoacetophenone → Ethanone, 1-[4-(2-propynylamino)phenyl]-
https://huagongshe.com/reaction/1722700
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | 3-Chloro-1-propyne | HCID 12221 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethanone, 1-[4-(2-propynylamino)phenyl]- | HCID 11469351 | 49% |
Reaction Steps
A mixture of 25 g (0.185 mol) of 4-aminoacetophenone, 12.7 ml (0.176 mol) of propargyl chloride, and 35 ml of diisopropylethylamine in 500 ml of dry toluene is stirred at 60° C. for eight hours then at 90° C. for twenty-four hours. The reaction is cooled to room temperature and poured into a saturated sodium bicarbonate solution. The organic portion is separated and concentrated in vacuo to an orange oil. The oil is chromatographed on silica gel eluting with a gradient of 20-50% ethyl acetate in hexane. The appropriate fractions are concentrated to leave a pale yellow solid. The solid is recrystallized from ethanol to give two crops of the desired product, 14.99 g (49% yield); mp 97°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857530 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-a05ca1d42dad4340929cc91936ca8f1e |
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| Source note | uspto-grants-1989_08 |
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