HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986623Generated: November 4, 2026
2-Mercaptobenzoic Acid → HCID 68865539, compound
https://huagongshe.com/reaction/1986623
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Mercaptobenzoic Acid | HCID 5443 | — |
| Reactant | HCID 68864592 | HCID 68864592 | — |
| Catalyst | 1,4-Bis(diphenylphosphino)butane | HCID 82124 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68865539 | HCID 68865539 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550467B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-a8185eccfe9040e29b86a949975cd7d4 |
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| Source note | uspto-grants-2009_06 |
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