HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 18058Generated: October 30, 2026
Sulfuric Acid → HCID 68586915, compound
https://huagongshe.com/reaction/18058
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22506676 | HCID 22506676 | — |
| Reactant | HCID 22506717 | HCID 22506717 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68586915 | HCID 68586915 | — |
Reaction Steps
1-(3-Methylsulfonylmethylphenyl)azetidine may be prepared by carrying out the procedure in the following manner: a solution of 1.9 g of 1-(3-methylsulfanylmethylphenyl)azetidine in 10 cm3 of ethanol is added to a mixture, cooled to 0° C., of 10 cm3 of water, 5 cm3 of acetic acid, 1.5 cm3 of 36 N sulfuric acid and 6.15 g of oxone. After stirring for 20 hours at 20° C., the reaction mixture is supplemented with 100 cm3 of water, 100 cm3 of ethyl acetate and is then neutralized by stirring with sodium hydrogen carbonate. The mixture obtained is separated after settling, the organic phase is dried over magnesium sulfate and then filtered and concentrated to dryness under reduced pressure (2.7 kPa). 1.55 g of 1-(3-methylsulfonyl-methylphenyl)azetidine are obtained in the form of a light brown gum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07741316B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-08c2fc198f4548609bed8b6b0ac4c2b7 |
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| Source note | uspto-grants-2010_06 |
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