HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 2',3'-Difluoro-4'-formylacetanilide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4'-Cyano-2',3'-difluoroacetanilide | HCID 14621039 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2',3'-Difluoro-4'-formylacetanilide | HCID 14621040 | 92.5% |
Reaction Steps
A mixture of 11 g of Raney nickel, 8.2 g of 4'-cyano-2',3'-difluoroacetanilide and 125 mL of 95% HCOOH is stirred and heated 30 minutes at 80°-85° C. The hot solution is filtered through diatomaceous earth and the cake washed with 3×100 mL of CH2CL2. The filtrate and wash are evaporated in vacuo to furnish a white solid. Excess saturated NaHCO3 is added to neutralize the residual HCOOH and the product is extracted with 3×400 mL of CH2Cl2. The CH2Cl2 extract is washed with saturated NaHCO3 and H2O (100 mL each), dried with Na2SO4 and evaporated to furnish 7.7 g (92.5% yield) of 2',3'-difluoro-4'-formylacetanilide, m.p. 154° C. The mass spectrum shows an ion at 200.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863959 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-1f1ae3f2f7f1464180de9126c4f03cc1 |
| Source note | uspto-grants-1989_09 |