HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 21265710, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 14888669 | HCID 14888669 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 88067715 | HCID 88067715 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Product | HCID 21265710 | HCID 21265710 | — |
Reaction Steps
To the compound of Example 33 (0.100 g, 0.189 mmol) in THF (0.90 mL) were added nBu4NI (catalytic) and a trace of 18-crown-6. To this mixture at −78° C. was added potassium tert-butoxide (1M in THF, 0.208 mL) after a period of 10 min at −78° C., a THF solution (0.30 mL) of tert-butyl 2-[4-(bromomethyl)phenyl]-2,2-difluoroacetate](0.066 g, 0.206 mmol) was added. After a period of 2 h, at 0° C., the reaction mixture was quenched as described for Example 31 Step 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06174874B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-4d010512c9ed495d9b6d46dbf2a5252a |
| Source note | uspto-grants-2001_01 |