HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827441Generated: October 30, 2026
Formic Acid → N-[2-Fluoro-4-(4-fluoro-benzyloxy)-phenyl]-2-formylamino-acetamide
https://huagongshe.com/reaction/1827441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-amino-N-[2-fluoro-4-(4-fluoro-benzyloxy)-phenyl]-acetamide | HCID 10447035 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | HCID 178506446 | HCID 178506446 | — |
| Product | N-[2-Fluoro-4-(4-fluoro-benzyloxy)-phenyl]-2-formylamino-acetamide | HCID 10336122 | 91% |
Reaction Steps
A mixture of acetic anhydride (40 mg, 0.39 mmol) and formic acid (22 mg, 0.48 mmol) was stirred at 0° C. and then heated uat 60° C. for 1 h. Step 2: During this time, 2-amino-N-[2-fluoro-4-(4-fluoro-benzyloxy)-phenyl]-acetamide (1:1) hydrochloride (50 mg, 0.15 mmol) was extracted with DCM and sodium hydrogen carboante (saturated) and the organic layer evaporated. Then to a mixture of the acetic formic anhydride (Step 1) in dry THF (0.5 mL) was added a solution of the amine (Step 2) in dry THF (1 mL) at room temperature and the resulting mixture stirred for 10 min. Then the reaction mixture was evaporated leave the title compound (44.1 mg, 91%) as a white solid. MS: m/e=321.1 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053245B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-b74e85e3a9fc467184f8d856fdd00454 |
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| Source note | uspto-grants-2006_05 |
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