HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448462Generated: November 1, 2026
Acetic Acid → 2-(5-Chloro-2-phenoxyphenyl)acetic acid
https://huagongshe.com/reaction/1448462
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(5-Chloro-2-phenoxyphenyl)-1-morpholinoethanethione | HCID 12765111 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(5-Chloro-2-phenoxyphenyl)acetic acid | HCID 12765114 | — |
Reaction Steps
To this morpholine residue is added 290 ml of glacial acetic acid, 61 ml of water and 87 ml of sulfuric acid (96%), and the mixture refluxed for a period of 21 hours. On cooling, the reaction mixture is dissolved in ethyl ether, washed with water until the water wash appears neutral and extracted with a 10% sodium carbonate solution. The aqueous alkaline layer is acidified with a 2 N solution of hydrochloric acid and re-extracted into diethyl ether. The ether solution is washed with water until the water washings are neutral, dried over anhydrous sodium sulfate and filtered. The solvent is removed by distillation from the filtrate and the remaining residue is crystallized from cyclohexane to yield 30.5 grams of (5-chloro-2-phenoxyphenyl)acetic acid having a m.p. of 119°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04180559 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-2e91b197024148eb809890fb6a4eb552 |
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| Source note | uspto-grants-1979_12 |
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