HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethoxyethane → HCID 59840902, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (2-(Benzyloxy)phenyl)boronic acid | HCID 2773253 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 59840902 | HCID 59840902 | 80% |
Reaction Steps
4,6-dichloropyrimidine (6.0 g, 40 mmol) and 2-benzyloxyphenylboronic acid (6.61 g, 29 mmol) were added to a solution of dimethoxyethane (120 mL) and water (18 mL), followed by the addition of NaHCO3 (6.72 g, 80 mmol) and (PPh3)2PdCl2 (0.84 g). To this end the reaction mixture was allowed to reflux for 8 h, and the solvent removed under reduced pressure. The residue was taken up in CH2Cl2 (100 mL), and the resulting solution washed with water, dried over anhydrous K2CO3, filtered and the solvent removed under reduced pressure. The crude product was purified by flash chropatography on silica gel (eluent CH2Cl2) and recrystallized from hexanes yielding 4-chloro-6-(2-benzyloxyphenyl)-pyrimidine (6.88 g; 80%) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08507498B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-afde9f49f0014af9b992587da4661fe2 |
| Source note | uspto-grants-2013_08 |