HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201763Generated: October 30, 2026
Hexacosanoic acid → HCID 117778469, compound
https://huagongshe.com/reaction/2201763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexacosanoic acid | HCID 10469 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 117778748 | HCID 117778748 | — |
| Solvent | HCID 23696006 | HCID 23696006 | — |
| Product | HCID 117778469 | HCID 117778469 | — |
Reaction Steps
(COCl)2 (2 mL) was added to hexacosanoic acid (139 mg, 0.39 mmol) and heated at 70° C. for 2 h, after which time the solution was cooled to rt, and the (COCl)2 removed under a stream of dry argon. The residual volatiles were removed under reduced pressure. The resulting crude acyl chloride was dissolved in THF (0.5 mL) and added with vigorous stirring to a solution of amine 72 (81 mg, 0.18 mmol) in THF/NaOAc(aq) (8M) (1:1, 2 mL). Vigorous stirring was maintained for 2 h, after which time the reaction mixture was left to stand and the layers were separated. The aqueous layer was extracted with THF (3×2.0 mL) and the organic layers were combined and concentrated under reduced pressure. The crude product was purified by column chromatography (10% MeOH in CHCl3) to give amide 73 as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09365496B2 |
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| Source dataset | uspto-grants-2016_06 |
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| ORD ID | ord-56ba5e9e259c46459fc7c9470c682c8e |
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| Source note | uspto-grants-2016_06 |
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