HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176377Generated: November 3, 2026
Acetic Anhydride → N-[2-(3-fluoro-2-hydroxyphenyl)ethyl]acetamide
https://huagongshe.com/reaction/1176377
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(3-Fluoro-2-hydroxyphenyl)acetonitrile | HCID 68499413 | — |
| Catalyst | Dichloronickel;hexahydrate | HCID 11791229 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-[2-(3-fluoro-2-hydroxyphenyl)ethyl]acetamide | HCID 68502069 | — |
Reaction Steps
A solution of 1.54 g of (3-fluoro-2-hydroxyphenyl)acetonitrile, 1.87 ml of acetic anhydride and 2.41 g of nickel chloride hexahydrate in 75 ml of methanol is admixed at 0° C. with 2.72 g of sodium borohydride in portions and stirred at room temperature over 22 hours. The reaction mixture is concentrated by evaporation, and the residue is diluted with ethyl acetate and saturated aqueous sodium bicarbonate solution and clarified by filtration. The aqueous phase is extracted with ethyl acetate (3×). The combined organic phases are dried with sodium sulphate and concentrated by evaporation. The title compound is obtained as a beige solid from the residue by means of flash chromatography (SiO2 60F). Rf=0.23 (95:5 dichloromethane-methanol); Rt=2.60.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07842688B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-cb1072cb16dd469882f979af86bc25f6 |
|---|
| Source note | uspto-grants-2010_11 |
|---|