HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341346Generated: October 30, 2026
Hydrochloric Acid → HCID 24771977, compound
https://huagongshe.com/reaction/341346
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Hydroxyacetophenone | HCID 8487 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 6-bromohexanoate | HCID 117544 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24771977 | HCID 24771977 | — |
Reaction Steps
A round bottom flask equipped with a magnetic stirrer bar and a reflux condenser was charged with 5.0 g (36.7 mmol) of 3-hydroxyacetophenone, 8.18 g (36.7 mmol) of ethyl 6-bromohexanoate and 50 mL of ethanol. The clear reaction mixture was treated with potassium carbonate (6.03 g, 44.0 mmol) and heated to reflux. After stirring for 24 hr at reflux, the reaction mixture was cooled to 25° C., filtered through a Celite pad and concentrated. The residue was taken up in of ethanol and treated with 15 mL of 2N aqueous sodium hydroxide (30 mmol). The reaction mixture was stirred for 6 hr at 25° C., before the ethanol was stripped off. The residue was acidified with aqueous 1N hydrochloric acid. The resulting solid was isolated by filtration and purified by recrystallization from ethanol/water to yield an off-white solid, 7.57 g, mp 70-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895777B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3b79f799df8546b180b2351e5773eafc |
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| Source note | uspto-grants-2014_11 |
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