Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 11-Dodecen-1-ol | HCID 520725 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 12-Methanesulfonyl-1-dodecene | HCID 23295897 | — |
Reaction Steps
To a solution of 11-dodecen-1-ol (5.5 g, 29.9 mmol) in dichloromethane (70 ml) at 0° C. was added methanesulfonyl chloride (3.55 g, 2.40 ml, 31.0 mmol) followed by triethylamine (4.38 g, 46.0 mmol). After stirring for 10 min at 0° C., the reaction was allowed to warm to 25° C. and stirred for 2 hr. The reaction was poured into water (60 ml), separated and washed with dichloromethane (50 ml). The organic portions were combined, dried (magnesium sulfate), and evaporated to give the 12-methanesulfonyl-1-dodecene as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05521315 |
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| Source dataset | uspto-grants-1996_05 |
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| ORD ID | ord-b6be420efe4346cb9ab796199f7df8f3 |
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| Source note | uspto-grants-1996_05 |
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