HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968181Generated: October 29, 2026
Dodecanoyl chloride → HCID 86759881, compound
https://huagongshe.com/reaction/968181
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dodecanoyl chloride | HCID 8166 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 86759882 | HCID 86759882 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86759881 | HCID 86759881 | — |
Reaction Steps
It was prepared exactly in a similar way as in the preparation of oleic acid N-hydroxy succinimide. In brief, 1.33 gr. of N-hydroxy succinimide (11.56 mmole, 1.5 eq.) and DIEA (1.35 ml) were dissolved in 50.0 ml of anhydrous THF and gently stirred at 0° C. under nitrogen atmosphere. Then, Lauroyl chloride (1.8 ml, 99% Sigma, 7.8 mmole, 1.0 eq.) dissolved in 50 ml of anhydrous THF was added dropwise during 1 h. The mixture was gently stirred for 2 h at 0° C. and over-night at room temperature. The resulting precipitate were discarded by filtration and the filtrate was evaporated under reduced pressure, redissolved in small amount of DCM and purified over silica-gel column using DCM as eluent. Fractions containing the product were combined and solvent was removed under reduced pressure. The resulting white solid was dried in vacuum over NaOH-pellets.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958325B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-331d805d375047b0a98becbc0f389acc |
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| Source note | uspto-grants-2005_10 |
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