HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192541Generated: October 31, 2026
Sodium Carbonate → 3-Oxocyclohex-1-en-1-yl trifluoromethanesulfonate
https://huagongshe.com/reaction/2192541
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Oxocyclohex-1-en-1-yl trifluoromethanesulfonate | HCID 10900851 | 67% |
Reaction Steps
To a solution of cyclohexane-1,3-dione (1 equiv) in DCM (0.4 M) was added Na2CO3 (1.0 equiv.) and cooled to 0° C. Added Tf2O (1.0 equiv.) in DCM (5 M) dropwise over 1 hr at room temperature under a nitrogen atmosphere. Upon addition, the reaction was stirred for 2 hr (dark red solution). The solution was filtered and to the filtrate was added saturated NaHCO3 (carefully), then extracted the organics, dried with brine, then Na2SO4, and concentrated. The crude was used for the next step without further purification. 3-oxocyclohex-1-enyl trifluoromethanesulfonate was obtained in 67% yield. The triflate decomposes upon storage and should be used immediately for the next reaction. LC/MS=244.9/286.0 (M+H and M+CH3CN); Rt=0.88 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329732B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-6e781f0029664cb2bf1013a061a9fce6 |
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| Source note | uspto-grants-2012_12 |
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