HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384814Generated: October 31, 2026
Hydrochloric Acid → 4-(2-Chloroethoxy)-3-methoxybenzoic acid
https://huagongshe.com/reaction/384814
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-(2-Chloro-ethoxy)-5-methoxy-benzoic acid methyl ester | HCID 23033016 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2-Chloroethoxy)-3-methoxybenzoic acid | HCID 22466671 | 96.4% |
Reaction Steps
In a 300 mL volume glass flask equipped with a stirrer, a thermometer and a dropping funnel were placed 17.40 g (69.7 mmol) of methyl 4-(2-chloroethoxy)-3-methoxybenzoate, 69.7 mL of aqueous sodium hydroxide solution (2 mol/L), and 69.7 mL of methanol. The resulting mixture was heated to 40° C. for 4 hours in an argon gas atmosphere. After the reaction was complete, the reaction mixture was cooled to 10° C., and neutralized by 69.7 mL of hydrochloric acid (2 mol/L). The reaction mixture was then placed to distill methanol off, and cooled to 10° C., to precipitate a crystalline product. The crystalline product was collected and dried under reduced pressure, to give 15.5 g (isolated yield: 95.2%, purity: 99% in terms of area percentage by high performance liquid chromatography) of 4-(2-chloroethoxy)-3-methoxybenzoic acid as a white crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367824B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-11e2d3978e81461bbf9af2c5c984e595 |
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| Source note | uspto-grants-2013_02 |
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