HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751036Generated: October 30, 2026
Water → N-(7-Cyano-2,3-dihydrobenzofuran-4-yl)-acetamide
https://huagongshe.com/reaction/751036
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | 4-Acetylamino-2,3-dihydrobenzofuran-7-carboxylic acid amide | HCID 68459409 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(7-Cyano-2,3-dihydrobenzofuran-4-yl)-acetamide | HCID 68459223 | 71.1% |
Reaction Steps
To a suspension of compound 4A (3.5 g, 16 mmol) in THF (64 mL) at 0° C. under Ar was added pyridine (6.5 mL, 80 mmol), followed by trifluoroacetic anhydride (5.6 mL, 40 mmol) dropwise. After addition, the reaction mixture was stirred at 0° C. for 5 min, then pored into H2O (50 mL), extracted with EtOAc (3×100 mL). The combined EtOAc extracts were washed with brine, dried (Na2SO4), and concentrated under reduced pressure to give a crude product, which was purified by crystallization from MeOH-EtOAc-Hexane to furnish the title compound (2.3 g) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07405234B2 |
|---|
| Source dataset | uspto-grants-2008_07 |
|---|
| ORD ID | ord-c05ecb52b26743fa92032e02d713728c |
|---|
| Source note | uspto-grants-2008_07 |
|---|