HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 4-(1H-Pyrrol-3-ylmethyl)-morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 4-(1-Triisopropylsilanyl-1H-pyrrol-3-ylmethyl)-morpholine | HCID 66636760 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(1H-Pyrrol-3-ylmethyl)-morpholine | HCID 57587018 | — |
Reaction Steps
To a solution of the compound obtained in Step A (75 mmoles) in THF (100 ml) there is added, dropwise, at 0° C., Bu4NF 1.0M in THF (75.0 mmoles). After stiffing at 0° C. for one hour, the solution is poured onto ice and is then extracted with DCM. The organic phases are combined and then washed with saturated aqueous NaCl solution, dried over sodium sulphate, filtered and evaporated to dryness to yield the title product, which is used directly in the next Step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653073B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-e634878a2a9d4cf187ed6a294a2f3208 |
| Source note | uspto-grants-2014_02 |