HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377761Generated: October 25, 2026
4-(Methylsulfonyl)benzaldehyde → HCID 70286603, compound
https://huagongshe.com/reaction/377761
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Methylsulfonyl)benzaldehyde | HCID 220376 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 5-methoxy-2-methyl-3-indenylacetate | HCID 53634864 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70286603 | HCID 70286603 | — |
Reaction Steps
25% methanolic sodium methoxide (16 ml, 2.0 equivalents) is treated with a solution of methyl 5-methoxy-2-methyl-3-indenylacetate (from Example 4, Part C) (8.7 g; 0.037 mol) and p-methylsulfonylbenzaldehyde, (6.3 g; 1.1 equivalent). The mixture is stirred at reflux under nitrogen for 2 hours. An equal volume of water is added slowly, and refluxing is continued for 30 min. The solution is cooled, is diluted with water and is washed with ether. Residual ether is blown off with nitrogen. The aqueous solution is acidified with 10% hydrochloric acid. The precipitated product is collected and is washed thoroughly with water. The crude product is crystallized from methanol to give (Z)-5-methoxy-2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenylacetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06028116 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-113586e271734fa8a1342d6dff985c0c |
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| Source note | uspto-grants-2000_02 |
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