HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217535Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 68807292, compound
https://huagongshe.com/reaction/2217535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | HCID 68805998 | HCID 68805998 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 68807292 | HCID 68807292 | — |
Reaction Steps
2-(3-Methyl-2′-methylsulfanyl-biphenyl-4-ylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.57 g, 1.3 mmol) was dissolved in 10 mL EtOAc, added m-chloroperoxybenzoic acid (1.76 g, 6.1 mmol) in one portion and stirred at ambient temperature for 3 hours. Reaction not complete. Concentrated and redissolved in 10 mL acetonitrile and added oxone (1.5 g, 2.4 mmol) in one portion and stirred at ambient temperature overnight and then concentrated. Redissolved in 100 mL EtOAc and 100 mL sat. NaHCO3, separated layers, washed organics with brine, dried with MgSO4, filtered and concentrated. Purified on a silica gel column eluted with 20% moving to 40% EtOAc in hexanes. Combined and concentrated pure fractions to yield title compound. (0.44 g, 72%) APCI (AP−): 457.1 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07407974B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-305aff75d00d4b3caed1b9445daff50e |
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| Source note | uspto-grants-2008_08 |
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