HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284460Generated: October 25, 2026
Triethylamine → 1-Docosanol, methanesulfonate
https://huagongshe.com/reaction/2284460
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Behenyl Alcohol | HCID 12620 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Docosanol, methanesulfonate | HCID 86650089 | — |
Reaction Steps
247.4 g of behenyl alcohol (1-docosanol) was dissolved in 640 mL of tetrahydrofuran, 116.1 mL of methanesulfonyl chloride was gradually added, and 64.7 mL of triethylamine was then added dropwise under ice cooling over 30 minutes. After stirring for one hour, the mixture was heated at 40° C. and further stirred for 30 minutes. The reaction mixture was poured into 3.5 L of ice water, and the resulting mixture was ultrasonically dispersed for 15 minutes and further stirred at room temperature for 4 hours. The dispersion was filtered under reduced pressure, and a crystal was washed with 2 L of water. The resulting white crystal was stirred in 1.5 L of acetonitrile for one hour, filtered under reduced pressure and then washed with 0.5 L of acetonitrile. The resulting crystal was dried under reduced pressure to obtain 303.4 g of a white crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145432B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-fc8dba8f6d8a441fa9d6889d44ee4d89 |
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| Source note | uspto-grants-2015_09 |
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