HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → HCID 20280077, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 20280073 | HCID 20280073 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20280077 | HCID 20280077 | 91.6% |
Reaction Steps
A mixture of formic acid (5.02 g) and acetic anhydride (11.14 g) was stirred for 30 minutes at 40° to 45° C. and cooled in an ice bath. To the cold mixed anhydride was added a solution of 3-(2-hydroxyethyl)aminopyridine (5.80 g) in tetrahydrofuran (20 ml) under cooling in an ice bath and stirring, which was continued for two hours at room temperature. The mixture was evaporated to remove tetrahydrofuran and poured into water (100 ml). The mixture was adjusted to pH 6 to 7 with sodium bicarbonate and extracted with methylene chloride. The extract was washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate and evaporated to give 3-[N-(2-formyloxyethyl)formamido]-pyridine (7.47 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04521413 |
| Source dataset | uspto-grants-1985_06 |
| ORD ID | ord-69f46a3271074eda82d3e10f4b4deba0 |
| Source note | uspto-grants-1985_06 |