HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414571Generated: October 27, 2026
Guaiacol → 5-Chloro-2-(2'-methoxyphenoxy)benzoic acid
https://huagongshe.com/reaction/1414571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Guaiacol | HCID 460 | — |
| Reactant | 2,5-Dichlorobenzoic acid | HCID 5784 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Chloro-2-(2'-methoxyphenoxy)benzoic acid | HCID 23460522 | — |
Reaction Steps
A mixture of 2,5-dichlorobenzoic acid (9.5 g.), 2-methoxyphenol (7.4 g.) and copper bronze (1.0 g.) is added to a solution of sodium methoxide in methanol prepared from sodium (2.53 g.) and methanol (50 ml.). The excess methanol is evaporated and 1,2-dichlorobenzene (50 ml.) is added to the residue. The mixture is stirred and heated under reflux for 2.5 hours. The mixture is cooled, acidified with 3N hydrochloric acid, filtered to remove copper bronze and extracted with chloroform. The organic layer is separated and extracted with saturated sodium hydrogen carbonate solution. The sodium hydrogen carbonate extract is acidified. The precipitate is filtered off, dissolved in toluene, and the toluene solution treated with carbon, filtered and the solvent evaporated. The solid residue is recrystallised from toluene-petroleum ether (b.p. 60°-80° C.) to give 5-chloro-2-(2'-methoxyphenoxy)benzoic acid, m.p. 115°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04001419 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-a5c8a006789446f0b0b26cf189c3d0d1 |
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| Source note | uspto-grants-1977_01 |
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