HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-3-chloropropane → 1-[(3-Chloropropyl)sulfanyl]-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Nitrobenzenethiol | HCID 15809 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[(3-Chloropropyl)sulfanyl]-4-nitrobenzene | HCID 14933055 | — |
Reaction Steps
1 g of potassium hydroxide is dissolved in 40 ml of methanol and mixed with 2.3 g of 4-nitrothiophenol. The suspension is stirred for one hour at room temperature and mixed drop by drop with 1.48 ml of 1-bromo-3-chloropropane. After 4 hours of stirring at room temperature, another 0.15 ml of 1-bromo-3-chloropropane is added in drops. The mixture is stirred for 65 hours at room temperature, concentrated by evaporation in a vacuum and taken up in ethyl acetate. It is extracted with water and saturated common salt solution, dried on sodium sulfate and concentrated by evaporation. After purification by flash chromatography, 2.54 g of 1-(3-chloro-propylsulfanyl)-4-nitro-benzene is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07338958B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-93ea9c15ad01461890548213e5dfeb86 |
| Source note | uspto-grants-2008_03 |