HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978570Generated: October 29, 2026
Sodium Thiosulfate → HCID 21995775, compound
https://huagongshe.com/reaction/1978570
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Methyl 7-(3,4-methylenedioxyphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate | HCID 18472255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21995775 | HCID 21995775 | — |
Reaction Steps
To a solution of methyl 7-(3,4-methylenedioxyphenyl)-2,3-dihydro-1-benzothiepine-4-carboxylate (0.80 g) in THF (10 ml) was added at 0° C. 70% 3-chloroperbenzoic acid (1.22 g), and the mixture was stirred at 0° C. for 15 minutes and then at room temperature for 2 hours. To the mixture was added an aqueous solution of sodium thiosulfate, and the mixture was stirred for a few minutes and extracted with dichloromethane. The organic layer was washed with sodium bicarbonate solution and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure to give solid, which was recrystallized from THF/isopropanol to give colorless crystals of methyl 7-(3,4-methylenedioxyphenyl)-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxylate (763.3 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235771B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-eaf4acc43b8a462893415ac448ba0e8a |
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| Source note | uspto-grants-2001_05 |
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