HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175747Generated: November 1, 2026
Boron trifluoride etherate → HCID 10562396, compound
https://huagongshe.com/reaction/2175747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1,2-Ethanedithiol | HCID 10902 | — |
| Reactant | Ethyl 4-oxocyclohexanecarboxylate | HCID 317638 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10562396 | HCID 10562396 | 75% |
Reaction Steps
To a stirred solution of ethyl 4-oxocyclohexane carboxylate (5 g, 29.41 mmol) and ethane-1,2-dithiol (4.14 g, 44.11 mmol) in DCM (25 mL) was added BF3.Et2O (4.17 g, 29.41 mmol) at 0° C. and the reaction mixture was allowed to stir at 20-35° C. for 2 h. Then the reaction mixture was rotary evaporated under vacuum to get residue which was purified by column chromatography using mixture of 5% ethyl acetate/hexane as an eluent to get the desired compound as a yellow liquid (5.4 g, 75%); 1H NMR (400 MHz, DMSO-d6) δ 4.05 (q, J=7.4 Hz, 2H), 3.34-3.26 (m, 4H), 2.42-2.34 (m, 1H), 2.10-2.02 (m, 2H), 1.96-1.84 (m, 4H), 1.66-1.54 (m, 2H), 1.17 (t, J=7.3 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062075B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-bc2cbd56dd4946d082c7cf77c9ddb37c |
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| Source note | uspto-grants-2015_06 |
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