HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Formate → Tert-butyl (5-formyl-2-methoxybenzyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | Tert-butyl (5-bromo-2-methoxybenzyl)carbamate | HCID 22926030 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | HCID 178418416 | HCID 178418416 | — |
| Product | Tert-butyl (5-formyl-2-methoxybenzyl)carbamate | HCID 22493931 | 75.1% |
Reaction Steps
1.015 g of t-butyl N-(5-bromo-2-methoxybenzyl)carbamate, 45 mg of dichlorobis(triphenylphosphine)palladium (II), 330 mg of sodium formate and 17 mg of triphenylphosphine were dissolved in anhydrous N,N-dimethylformamide, followed by stirring for 2 hours at 110° C. in carbon monoxide atmosphere. The reaction mixture was diluted with ethyl acetate, and washed with water and saturated sodium bicarbonate water. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated. The residue was purified by silica gel column chromatography, and 640 mg of t-butyl N-(5-formyl-2-methoxybenzyl)carbamate was obtained from fractions eluted with hexane-ethyl acetate (3:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244861B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-04a0c5bca7cd4ea2a1e72ff93846ae5a |
| Source note | uspto-grants-2007_07 |