HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]formamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 3-Methoxy-4-hydroxyphenylethylamine hydrochloride | HCID 11957621 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]formamide | HCID 11389958 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Formic acid (230 g, 5.0 mol) is added dropwise to acetic anhydride (383 g, 3.75 mol) at 0° C. This mixture is stirred for 2 hours at +55° C. and subsequently cooled again to 0° C. Tetrahydrofuran (500 ml) is added at this temperature followed by 4-(2-amino-ethyl)-2-methoxyphenol hydrochloride (50 g, 0.25 mol). The resulting white suspension is stirred for 18 hours at +75° C., changing into a yellow solution. The reaction mixture is evaporated and the residue is submitted to flash-chromatography to yield N-[2-(4-hydroxy-3-methoxy-phenyl)-ethyl]-formamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700522B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-c5b198bb6b904bea99200b2f7d29f02c |
| Source note | uspto-grants-2010_04 |