HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1488442Generated: October 26, 2026
Potassium Hydroxide → HCID 22904614, compound
https://huagongshe.com/reaction/1488442
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Isopropyl bromoacetate | HCID 121593 | — |
| Reactant | 3-(1,3-Dioxolan-2-yl)aniline | HCID 7020362 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Product | HCID 22904614 | HCID 22904614 | — |
Reaction Steps
165.19 g (1.00 mol) of 2-(3-aminophenyl)-1,3-dioxolan (CA 108 (15): 131815 r), 156.35 g (3.00 mol) of pulverized potassium hydroxide and 11.39 g (0.05 mol) of benzyltriethylammonium chloride are vigorously mechanically stirred under argon and heated to 80° C. 543.09 g (3.00 mol) of bromoacetic acid isopropyl ester is instilled in the suspension and the reaction mixture is stirred for about 8 hours at 80° C. Then, it is filtered, the filtrate is shaken out several times with concentrated aqueous sodium bicarbonate solution, the organic phase is dried on anhydrous magnesium sulfate, filtered and concentrated by evaporation in a vacuum. The residue is chromatographed on silica gel 60 (Merck) with methylene chloride/methanol. After concentration by evaporation, the product fractions yield a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05674467 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-414ae294111346948c54c9e7c768afca |
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| Source note | uspto-grants-1997_10 |
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