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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955717Generated: October 31, 2026

m-Chloroperbenzoic acid → HCID 53697930, compound

https://huagongshe.com/reaction/1955717

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 53670423HCID 53670423—
SolventAcetoneHCID 180—
ProductHCID 53697930HCID 53697930—

Reaction Steps

A solution of sodium periodate, 4.28 g (20 mol) in 40 ml of water is added dropwise to 6-fluoro-5-methoxy-2-methyl-1-(p-methylthiobenzylidene)-3-indenylacetic acid, 3.70 g (10 mmol) in 300 ml methanol and enough acetone to cause solution. This solution is stirred overnight at room temperature and filtered. The filtrate is evaporated at 30° to a small volume which causes the product to precipitate. The suspension is diluted with several volumes of water, and is cooled. Collected crystals are washed with water and methanol-water (1:1). The product is dried in vacuo over potassium hydroxide pellets and then in a vacuum oven at 70° C. The crude product is recrystallized from methylene chloride-petroleum ether to give 6-fluoro-5-methoxy-2-methyl-1-(p-methylsulfinyl-benzylidene)-3-indenylacetic acid (m.p. 190°-193°). 6-fluoro-5-methoxy -2-methyl-1-(p-methylsulfonylbenzylidene)-3-indenylacetic acid is prepared according to the procedure of Example 1, part G by the addition of 1.0 mol of m-chloroperbenzoic acid per mol of 6-fluoro-5-methoxy-2-methyl-1-(p-methylsulfinylbenzylidene)-3-indenyl acetic acid in an acetone solution.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05776962
Source datasetuspto-grants-1998_07
ORD IDord-b5e9fac20ffa4ec381a31813a9ee12a7
Source noteuspto-grants-1998_07