HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 2-Fluoro-5-(hydroxymethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(Bromomethyl)-2-fluorobenzonitrile | HCID 2773931 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 2-Fluoro-5-(hydroxymethyl)benzonitrile | HCID 2773934 | — |
Reaction Steps
A solution of 85% formic acid (0.63 mL) and triethylamine (2.32 mL, 16.7 mmol) in acetonitrile at 0° C. was treated with the product from Example 82A (1.3 g, 5.6 mmol), stirred at room temperature for 3 hours, the reaction evaporated to dryness, partitioned between ethyl acetate/water, the organic layer dried with sodium sulfate, filtered and solvent evaporated to provide a crude formate ester. This residue was dissolved in methanol:water (5:1), treated with a catalytic amount of concentrated hydrochloric acid, stirred at room temperature overnight, evaporated to dryness, and flash chromatographed over silica gel eluting with ethyl acetate:hexane (1:1) to provide 0.40 g 3-cyano-4-fluorobenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265417B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-70f73e46840f42318450eab35c65ac06 |
| Source note | uspto-grants-2001_07 |