HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307133Generated: November 1, 2026
Acetone → (+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanecarboxylic Acid
https://huagongshe.com/reaction/2307133
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetone | HCID 180 | — |
| Reactant | (+/-)-{3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexyl}methanol | HCID 22337773 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | (+/-)-3-[2,4-Bis(methoxymethoxy)phenyl]cyclohexanecarboxylic Acid | HCID 22337771 | 29% |
Reaction Steps
A solution of (±)-{3-[2,4-bis(methoxymethoxy)phenyl]cyclohexyl}methanol (50 mg) in acetone (1 ml) was added to a stirred solution of chromium (VI) oxide (64 mg) in 2M sulfuric acid (0.64 ml) at 0° C. over 3 hr. After 3 hr at 0° C. and then 16 hr at room temperature, the reaction mixture was partitioned between water (10 ml) and ethyl acetate (20 ml). The layers were separated and the aqueous layer was extracted with ethyl acetate (2×20 ml). The combined organic extracts were washed with water (20 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, ethyl acetate/petrol, 4:1 v/v) to give the title compound as a colourless oil (15 mg, 29%). Rf (ethyl acetate/petrol, 4:1 v/v) 0.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06828460B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-6e415ce63f4f4d79a9dbc367f17969be |
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| Source note | uspto-grants-2004_12 |
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