HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2-(Bromomethyl)-5-(2'-methoxy-5'-fluorobenzyl)tetrahydrofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-(2'-Methoxy-5'-fluorophenyl)hex-5-en-2-ol | HCID 67499476 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Bromomethyl)-5-(2'-methoxy-5'-fluorobenzyl)tetrahydrofuran | HCID 67499060 | — |
Reaction Steps
To a solution of 1-(2′-methoxy-5′-fluorophenyl)hex-5-en-2-ol (1.35 g, 6.0 mmol) in dry CH2Cl2 (30 mL) at 0° C. was added N-bromosuccinimide (NBS, 1.30 g, 7.2 mmol) portionwise and the reaction was warmed to room temperature for 12 h. Solvent was then removed in vacuo and the residue was purified by flash column chromatography (5% EtOAc in Hexane, Rf=0.12) to give in the trans isomer (663 mg, 36%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168635B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-9b571283749b408aa76744aecb83cfbb |
| Source note | uspto-grants-2012_05 |