Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 53688373 | HCID 53688373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 54130451 | HCID 54130451 | — |
Reaction Steps
To 1-tetrahydropyranyloxy-1-[2-(4-fluorophenylthio)phenyl]prop-2-ene (2.71 g; 7.87 mmol) in 20 ml of diethyl ether under nitrogen cooled in an ice bath, was added concentrated HBr and the mixture stirred at 0° C. for one hour. The ice bath was removed and the reaction mixture stirred at room temperature overnight. The reaction mixture was poured into water and extracted twice with hexane. The organics were collected and washed with water and then brine and dried over MgSO4 and concentrated to afford the subtitle compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05283361 |
|---|
| Source dataset | uspto-grants-1994_02 |
|---|
| ORD ID | ord-28e3f820184641c7b39a5722eb7ddfca |
|---|
| Source note | uspto-grants-1994_02 |
|---|