HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethyloxonium tetrafluoroborate → HCID 21200268, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| Reactant | HCID 6461349 | HCID 6461349 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21200268 | HCID 21200268 | — |
Reaction Steps
Under an atmosphere of argon 11.36 g of 3-benzyloxybenzamide were suspended in CH2Cl2 (200 ml) and 9.5 g triethyloxonium fluoroborate in CH2Cl2 (100 ml) were added dropwise on ice cooling. The reaction mixture was then stirred further 20 h at RT until completion of reaction according to TLC analysis (CH2Cl2/MeOH: 15/1). The solid which had formed was filtered off, washed with ether to give the desired ethyl m-benzyloxybenzimidate tetrafluoroborate as white crystals, mp 152°-154° C., which was used without further purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06242601B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-f0cc0210d5be42109de96a78f3e0b793 |
| Source note | uspto-grants-2001_06 |