HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-(4,4'-Dimethoxytrityloxy)methyl-5-fluoromethylbenzylazide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | 3-Azidomethyl-5-fluoromethylbenzylalcohol | HCID 86671518 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(4,4'-Dimethoxytrityloxy)methyl-5-fluoromethylbenzylazide | HCID 86671519 | — |
Reaction Steps
From a reaction system containing 3-Azidomethyl-5-fluoromethylbenzylalcohol (36) (142 mg, 0.73 mmol), the air was evacuated and then Ar was charged therein. To this were added DMTrCl (323 mg, 0.95 mmol), DMF (2.0 mL), and pyridine (2.0 mL), and stirred for 22 hours at a room temperature. TLC was used to confirm the progress of the reaction. Then, the solvent was removed in vacuo. The residue was subjected to extraction with EtOAc. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous sodium sulfate, and evaporated under reduced pressure to remove the solvent. The residue was purified by neutral silica gel column chromatography (hexane:EtOAc=20:1 to 5:1) to isolate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633304B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-47430a3c2d1a4af5b8a28ed05ff37a15 |
| Source note | uspto-grants-2014_01 |