HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380706Generated: October 31, 2026
4-Methoxyphenylacetic Acid → Manganese chloride (MnCl2), monohydrate
https://huagongshe.com/reaction/380706
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxyphenylacetic Acid | HCID 7690 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Manganese(2+) dichloride | HCID 10313134 | — |
| Product | Manganese chloride (MnCl2), monohydrate | HCID 18365734 | — |
| Product | Sodium Phenylacetate | HCID 23690424 | — |
Reaction Steps
Turning now to FIG. 1, a four step synthetic route for the preparation of α,δ-bis(4-hydroxy)sexiphenylene, in accordance with an embodiment of the present invention, is presented. Thus in a first step, a first solution is prepared by adding an appropriate amount of 4-methoxyphenylacetic acid to an aqueous solution of sodium carbonate. To this first solution is added an appropriate amount of a second solution, aqueous manganese chloride, to produce a pink foamy mixture. This mixture is washed with water and filtered to yield a pink powder, now comprising sodium phenylacetate and manganese dichloride hydrate. This pink powder is distilled at 300-320° C. under vacuum to effect a thermally induced dehydrative coupling reaction to give an excellent yield (72%) of white crystals of 1,3-bis(4-methoxyphenyl)propanone, having a melting point of between approximately 75-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06303733B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-7b8c29d8226e4f6fa6c9a7a36ee52048 |
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| Source note | uspto-grants-2001_10 |
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