HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656934Generated: October 30, 2026
Hydrochloric Acid → N-(3,5-difluorophenyl)-3,3-bis(methyloxy)propanamide
https://huagongshe.com/reaction/656934
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5-Difluoroaniline | HCID 96595 | — |
| Reactant | Methyl 3-methoxyprop-2-enoate | HCID 2724617 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(3,5-difluorophenyl)-3,3-bis(methyloxy)propanamide | HCID 68811062 | 126% |
Reaction Steps
A solution of 3,5-difluoroaniline (5 g, 38.8 mmol), methyl-3-methoxyacrylate (4.6 ml, 42.7 mmol) and sodium methoxide solution (25% in MeOH, 12 ml) in toluene (50 ml) under Argon was stirred at 70° C. for 3 h. More sodium methoxide solution (25% in MeOH, 6 mL) added and reaction stirred overnight. Still more sodium methoxide solution (25% in MeOH, 12 mL) and methyl-3-methoxyacrylate (5 mL, 46.4 mmol) were then added and reaction was heated at 70° C. for 5 h. MeOH was added and volume of toluene was reduced to about 10 ml. The residue was acidified to pH 7 using a saturated solution of ammonium chloride, solid ammonium chloride and 5N HCl. The aqueous phase was extracted using ethyl acetate (2×500 ml). The combined organic phases were dried, evaporated and the residue was chromatographed on silica gel, eluting with 0-100% ethyl acetate-40-60° C. petroleum ether to afford the impure desired compound (12 g, 126%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071592B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-896f8d997f37489995025d3895b6ec80 |
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| Source note | uspto-grants-2011_12 |
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