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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238992Generated: October 29, 2026

2-Mercaptobenzoic Acid → HCID 68951149, compound

https://huagongshe.com/reaction/238992

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Mercaptobenzoic AcidHCID 5443—
ReactantHCID 23414403HCID 23414403—
ReactantHCID 68950383HCID 68950383—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68951149HCID 689511493.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642642B2
Source datasetuspto-grants-2014_02
ORD IDord-cf6bcb019d1c4892a125bae3369a0be1
Source noteuspto-grants-2014_02