HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389686Generated: October 29, 2026
Benzyl mercaptan → 1-(3-Benzylsulfanyl-2-fluoro-phenyl)-pyrrolidin-2-one
https://huagongshe.com/reaction/389686
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl mercaptan | HCID 7509 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | HCID 67155260 | HCID 67155260 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(3-Benzylsulfanyl-2-fluoro-phenyl)-pyrrolidin-2-one | HCID 67155414 | — |
Reaction Steps
Intermediate 98 (1.48 g, 5.73 mmol) in dioxane (50 ml) was stirred under argon. DIPEA (2 ml, 11.47 mmol), xantphos (0.2 g, 0.34 mmol) and Pd2(dba)3 (0.157 g, 0.17 mmol) were added and the reaction was heated to 100° C. Phenyl-methanethiol (0.64 ml, 5.45 mmol) was slowly added and the reaction stirred for 1 h. The reaction was quenched by the addition of 50 ml of H2O. After extraction with ethyl acetate (three times) the combined organic layers were washed with water, dried with Na2SO4, evaporated to dryness and the product was purified by silica gel chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08378092B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-c2860cbdf4814a9ab7a1f5d279200616 |
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| Source note | uspto-grants-2013_02 |
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