HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethyl [4-(tetrahydropyran-4-ylsulfanyl)phenyl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-iodotetrahydro-2H-pyran | HCID 2795506 | — |
| Reactant | 4-Mercapto-phenyl-acetic acid ethyl ester | HCID 12330043 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl [4-(tetrahydropyran-4-ylsulfanyl)phenyl]acetate | HCID 58860815 | — |
Reaction Steps
NEt3 (1.3 mL, 9.0 mmol) and 4-iodotetrahydropyran (1.93 g, 9.0 mmol) were added to a stirred solution of ethyl(4-mercaptophenyl)acetate (1.21 g, 6.0 mmol) in anhydrous DMF (10 mL) at 0° C. The mixture was allowed to warm to room temperature over 3 d, then the solvents were removed under reduced pressure. The residue was partitioned between Et2O (100 mL) and saturated aqueous NH4Cl (50 mL), the aqueous phase being extracted further with Et2O (45 mL). The combined ethereal extracts were washed with H2O (50 mL), H2O-saturated aqueous Na2CO3 (1:1, 50 mL), and brine (50 mL), before being dried (MgSO4). Filtration, solvent evaporation, and flash chromatography (IH-Et2O, 10:1 to 2:1) afforded the title compound: RF (IH-Et2O, 2:1)=0.31.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582632B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-7a710407978a4f4287ad8295cf4d02bb |
| Source note | uspto-grants-2009_09 |