HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096921Generated: October 28, 2026
Trifluoroacetic acid → HCID 23648567, compound
https://huagongshe.com/reaction/2096921
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 57539234 | HCID 57539234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23648567 | HCID 23648567 | 77.2% |
Reaction Steps
Tert-Butyl {(1R)-2-(benzylamino)-1-[(difluoromethoxy)methyl]-2-oxoethyl}carbamate (340 mg, 0.987 mmol) was stirred with trifluoroacetic acid (2.25 mL) and dichloromethane (2.5 mL) in an ice bath for an hour. The reaction mixture was concentrated, stirred with acetic anhydride-pyridine (1:1, 5.8 mL) at room temperature for 30 minutes and then diluted with ethyl acetate, washed with saturated sodium bicarbonate, brine, 0.5N HCl and brine again. The organic layer was dried, concentrated, and triturated with diethyl ether to give (2R)-2-(acetylamino)-N-benzyl-3-(difluoromethoxy)propanamide (230.5 mg, 77.2%) as a white solid. Mp: 186.9° C. 1H NMR (300 MHz, DMSO-d6): (ppm) 8.60 (t, 1H), 8.30 (d, 1H), 7.28-7.45 (m, 5H), 6.67 (wt, 1H), 4.58 (m, 1H), 4.40 (d, 2H), 3.98 (d, 2H) and 1.88 (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-fa0ad3e7c5324f838573e4556aa8c218 |
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| Source note | uspto-grants-2013_05 |
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