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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986623Generated: November 4, 2026

2-Mercaptobenzoic Acid → HCID 68865539, compound

https://huagongshe.com/reaction/1986623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Mercaptobenzoic AcidHCID 5443—
ReactantHCID 68864592HCID 68864592—
Catalyst1,4-Bis(diphenylphosphino)butaneHCID 82124—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68865539HCID 68865539100%

Reaction Steps

To a solution of (2S,5R)-1-allyl-4-(3-chloro-propyl)-2,5-dimethyl-piperazine (14.05 g, 61 mmol) in anhydrous THF (78 mL) under argon was added thiosalicylic acid (10.33 g, 67 mmol, 1.1 eq) followed by the addition of a solution of tris(dibenzylidenacetone)-dipalladium (Pd2(dba)3, 2.8 g, 3.1 mmol, 5 mol %) and 1,4-bis(diphenylphosphino)butane (DPPB, 1.33 g, 3.1 mmol, 5 mol %) in anhydrous THF (26 mL, pre-mixed for 15 minutes). After stirring at room temperature for 2 hours, the mixture was filtered through Celite. The filtrate was concentrated in vacuo and the residue was partitioned between 1N aqueous HCl (70 mL) and Et2O (70 mL). The aqueous layer was separated and extracted with Et2O (50 mL×2), and treated with NaOH (solid) to bring its pH to 13. The aqueous phase was extracted with CHCl3 (50 mL×4). The combined organic phase was dried (Na2SO4) and concentrated in vacuo to give 11.6 g (100%) of (2S,5R)-4-(3-chloro-propyl)-2,5-dimethyl-piperazine as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550467B2
Source datasetuspto-grants-2009_06
ORD IDord-a8185eccfe9040e29b86a949975cd7d4
Source noteuspto-grants-2009_06