Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Butyn-1-ol | HCID 12991 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 11051825 | HCID 11051825 | 100% |
Reaction Steps
2-Butyne-1-ol (1.4 g, 20 mmol) is dissolved in ether (50 mL) and cooled to 0° C. Triethylamine (3.3 mL, 24 mmol) is added to the solution. Methanesulfonyl chloride (1.6 mL, 22 mmol) is dissolved in ether (5 mL) and added dropwise to the reaction solution. The mixture is stirred for 30 minutes at 0° C., then filtered and concentrated to give crude methanesulfonic acid but-2-ynyl ester 20 (2.96 g, 20 mmol, quant.) as a colorless liquid: 1H-NMR (400 MHz, CDCl3) δ=4.79 (q, J=2.4 Hz, 2H), 3.08 (s, 3H), 1.87 (t, J=2.4 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820705B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-b1b3edaf26f4427baf3b3fa533ea63da |
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| Source note | uspto-grants-2010_10 |
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