HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013607Generated: October 31, 2026
m-Fluorobenzenethiol → HCID 59207197, compound
https://huagongshe.com/reaction/1013607
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Fluorobenzenethiol | HCID 75710 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Reactant | 3-Hydroxyazetidine | HCID 1514290 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Ammonium Hydroxide | HCID 14923 | — |
| Product | HCID 59207197 | HCID 59207197 | 465.9% |
Reaction Steps
In 5 mL dioxane under argon was mixed 1-(R)-6-Iodo-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl)-azetidin-3-ol (0.172 g, 0.5 mmol), tris(dibenzylideneacetone)-dipalladium(0) (0.023 g, 0.025 mmoles), 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (0.029 g, 0.05 mmol), diisopropylethyl amine (1 mmol) and 3-fluoro-thiophenol (0.13 g, 1.0 mmoles). The reaction mixture was stirred at 60° for 45 minutes, then was cooled and diluted with EtOAc. The organic layer was washed 1.5 M aqueous sodium carbonate, dried (magnesium sulfate), filtered and concentrated under reduced pressure. The residue was subjected to preparative HPLC (hexanes/EtOAc 1:1 to 50% hexanes/27% EtOA/15% MeOH/8% con. NH4OH) to give 0.08 g (47%) of 1-[(R)-6-(3-fluoro-phenylsulfanyl)-1,2,3,4-tetrahydro-naphthalen-1-ylmethyl]-azetidin-3-ol, MS M+H=344.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981923B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-3a2da11406f54aeba454317d1f7c9de6 |
|---|
| Source note | uspto-grants-2011_07 |
|---|