HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2-Methoxycarbonylthiophen-3-ylmethyltriphenylphosphonium bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Methyl 3-(bromomethyl)thiophene-2-carboxylate | HCID 10537693 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methoxycarbonylthiophen-3-ylmethyltriphenylphosphonium bromide | HCID 19693052 | 70.4% |
Reaction Steps
To a solution of methyl 3-bromomethyl-2-thiophenecarboxylate (7.31 g, 31.1 mmol) in toluene (90 ml) was added triphenylphosphine (7.92 g, 30.2 mmol) under ice cooling. The temperature of the mixture was raised to room temperature, followed by stirring for 2 days. The precipitated crystals were collected by filtration and dried to give 2-methoxycarbonylthiophen-3-ylmethyltriphenylphosphonium bromide (10.57 g, 70.4%). This product was subjected to the reaction of Reference Example 13 without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05726325 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-f5ea82e1d125454e8bce94b7fc33917f |
| Source note | uspto-grants-1998_03 |