HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306466Generated: October 25, 2026
Hydrochloric Acid → N-[11-(3-fluoro-4-methoxy-phenyl)-11-oxo-undecyl]acetamide
https://huagongshe.com/reaction/2306466
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Fluoroanisole | HCID 67576 | — |
| Reactant | 11-Acetamidoundecanoic acid | HCID 454085 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 11-Acetylamino-undecanoyl chloride | HCID 18434292 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[11-(3-fluoro-4-methoxy-phenyl)-11-oxo-undecyl]acetamide | HCID 18434110 | 107.7% |
Reaction Steps
0.5 ml of oxalyl chloride is added to a solution of 1.2 g of 11-acetylamino-undecanoic acid and 5 drops of DMF in 15 ml of methylene chloride at 0° C. and the mixture is stirred at RT for 3 hrs. The solution of the 11-acetylamino-undecanoyl chloride is treated under argon with 0.6 g of 2-fluoroanisole, cooled to −15° C. and treated with 1.4 g of aluminium chloride. After 2 hrs. at −15° C. the mixture is left to warm to room temperature overnight. The solution is treated with 15 ml of 1M hydrochloric acid at 0° C. and then with 20 ml of water. The organic phase is separated and washed with 1M hydrochloric acid, with water and with saturated sodium bicarbonate solution, dried and concentrated. 1.8 g of N-[11-(3-fluoro-4-methoxy-phenyl)-11-oxo-undecyl]acetamide are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06441177B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-84ac9039dd8d4cddb08ba3c2cbfb5fac |
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| Source note | uspto-grants-2002_08 |
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