HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114016Generated: October 30, 2026
Oxalyl chloride → 2-(4-Fluorophenyl)acetyl isocyanate
https://huagongshe.com/reaction/2114016
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-(4-Fluorophenyl)acetamide | HCID 573120 | — |
| Reactant | Methyl 2-(4-fluorophenyl)acetylcarbamate | HCID 21081725 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 2-(4-Fluorophenyl)acetyl isocyanate | HCID 23153088 | — |
Reaction Steps
To a solution/suspension of 4-fluorophenylacetamide (77 mg, 0.50 mmol, see generally, J. Med. Chem. 2003, 46, 4333-4341, the disclosure of which is herein incorporated by referene) in dichloroethane (2 mL) was added oxalyl chloride (0.175 mL, 2.00 mmol). The reaction was heated at 80° C. for 24 h and then 70° C. for two days. By this time, most of the solids had dissolved and the reaction was yellow. LC/MS analysis found a peak with a molecular weight of 211 corresponding to methyl 2-(4-fluorophenyl)acetylcarbamate, resulting from quenching of the isocyanate with methanol. The reaction was concentrated in vacuo to give a yellow slurry. The slurry was redissolved in dichloroethane (2 mL) and again concentrated in vacuo. The resulting residue was redissolved again in dichloroethane (2 mL) to give a 0.25 M solution of 2-(4-fluorophenyl)acetyl isocyanate in dichloroethane, which was used directly in subsequent reactions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07432373B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-4b3ef6bbb10f436e80743ad1b9713f27 |
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| Source note | uspto-grants-2008_10 |
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