HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis(2-chloroethyl) ether → 4-(3-(trifluoromethyl)phenyl)tetrahydro-2H-pyran-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis(2-chloroethyl) ether | HCID 8115 | — |
| Reactant | m-Trifluoromethylphenylacetonitrile | HCID 75360 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-(trifluoromethyl)phenyl)tetrahydro-2H-pyran-4-carbonitrile | HCID 43119034 | 162.8% |
Reaction Steps
Potassium tert-butoxide (4.00 g, 35.6 mmol, 2.20 eq) was added to a stirred solution of 2-(3-(trifluoromethyl)phenyl)acetonitrile (2.53 mL, 16.2 mmol, 1.0 eq) in DMF (30 mL) at 0° C. under a nitrogen atmosphere. The mixture was stirred for 10 minutes at 0° C. before 1-chloro-2-(2-chloroethoxy)ethane (2.09 mL, 17.8 mmol, 1.1 eq) was added dropwise via syringe. The reaction mixture was allowed to warm to room temperature and stirred for 6 hours. The reaction mixture was then cooled to 0° C. and quenched with 10% HCl. The aqueous mixture was extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), and concentrated in vacuo to give the product as an orange oil (6.73 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928139B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-5ed30b8c85f64632a39b32faf2919740 |
| Source note | uspto-grants-2011_04 |