HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096926Generated: October 31, 2026
Acetic Anhydride → 2-acetylamino-N-benzyl-3-difluoromethoxy-propionamide
https://huagongshe.com/reaction/2096926
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 23649017 | HCID 23649017 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-acetylamino-N-benzyl-3-difluoromethoxy-propionamide | HCID 23649016 | 59.1% |
Reaction Steps
2-Amino-N-benzyl-3-difluoromethoxy-propionamide (195 mg, 0.80) was mixed with triethylamine (322 mg, 3.19 mmol) in THF (5 mL). Acetic anhydride (98.5 mg, 0.96 mmol) was then added and the reaction mixture was stirred for 1 hour. The mixture was then diluted with ethyl acetate and washed with water. The organic layer was dried and concentrated. The residue was purified by column chromatography using hexanes:ethyl acetate (50:50 to 0:100). The isolated product was triturated with diethyl ether to give 2-acetylamino-N-benzyl-3-difluoromethoxy-propionamide (135 mg, 59%) as a white solid. 1H NMR (300 MHz, CDCl3): δ (ppm) 7.33 (m, 5H), 6.68 (br, 1H), 6.37 (br, 1H), 6.24 (t, 1H), 4.72 (q, 1H), 4.87 (d, 2H), 4.23 (dd, 1H), 4.01 (dd, 1H), 2.05 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450336B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-1307a85cfc8c4372bcb2a3a41416066c |
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| Source note | uspto-grants-2013_05 |
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