HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 59456303, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | [5-(4-Triisopropylsilanyloxyphenyl)selenophen-2-yl]-methanol | HCID 86644792 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59456303 | HCID 59456303 | — |
Reaction Steps
8.7 g (21.4 mmol) of [5-(4-triisopropylsilanyloxyphenyl)selenophen-2-yl]-methanol are initially introduced in 200 ml of THF, and 50 ml of TBAF (50 mmol, 1 M soln. in THF) are added with ice-cooling. After 30 min at this temperature, the mixture is added to water and extracted with MTBE. The organic phase is separated off, and the aqueous phase is extracted with MTBE. The combined organic phases are washed with sat. sodium chloride soln. and dried using sodium sulfate. The solution is concentrated to dryness, and the residue is recrystallised from ethyl acetate. 4-(5-Hydroxymethylselenophen-2-yl)phenol is obtained as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08304036B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-c7d5dc7d917d420ca1d23f2ed75fa568 |
| Source note | uspto-grants-2012_11 |