HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238992Generated: October 29, 2026
2-Mercaptobenzoic Acid → HCID 68951149, compound
https://huagongshe.com/reaction/238992
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptobenzoic Acid | HCID 5443 | — |
| Reactant | HCID 23414403 | HCID 23414403 | — |
| Reactant | HCID 68950383 | HCID 68950383 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68951149 | HCID 68951149 | 3.5% |
Reaction Steps
0.071 g of tris-(dibenzylidenaceton)-dipalladium(0) (0.08 mmol) and 0.033 g of 1,3-bis-(diphenylphosphino)-butane (0.08 mmol) were dissolved in 20 ml tetrahydrofurane and stirred for 30 min. 0.32 g of N-[4-((S)-1-allyl-pyrrolidin-3-yl)-phenyl]-3-trifluoromethyl-benzenesulfonamide (0.78 mmol), dissolved in 5 ml tetrahydrofurane, were added to the solution, followed by 0.129 g 2-mercaptobenzoic acid (0.84 mmol). The reaction mixture was stirred at room temperature for 72 h, the solvent was evaporated, and dichloromethane and 1 N aqueous hydrochloric acid were added. The aqueous phase was adjusted to basic pH, extracted with dichlormethane and the combined organic layers were washed with aqueous sodium chloride solution, dried over sodium sulphate, filtered and evaporated to dryness under reduced pressure. The crude product was purified via silica gel chromatography using a ISCO companion instrument to yield 0.01 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642642B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-cf6bcb019d1c4892a125bae3369a0be1 |
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| Source note | uspto-grants-2014_02 |
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