HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-[(3-Ethynylphenyl)amino]ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 89397433 | HCID 89397433 | — |
| Product | 2-[(3-Ethynylphenyl)amino]ethanol | HCID 28564219 | — |
Reaction Steps
N-(2-{[tert-Butyl(dimethyl)silyl]oxy}ethyl)-3-ethynylaniline (335 mg, 1.22 mmol) was treated with 1M TBAF in THF (1.5 mL, 1.5 mmol) at room temperature for 5 min. The volatiles were removed and the crude was dissolved in EtOAc (30 mL). The organic phase was washed with water (20 mL) and finally with brine, dried over sodium sulfate and evaporated to give the corresponding alcohol as brownish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08912200B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-873eefa3c19a485e8db91fe06883c83a |
| Source note | uspto-grants-2014_12 |