HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butyne-1,4-diol → HCID 178501074, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butyne-1,4-diol | HCID 8066 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178501086 | HCID 178501086 | — |
| Catalyst | HCID 178420236 | HCID 178420236 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178501074 | HCID 178501074 | 69% |
Reaction Steps
To a mixture of trans-methyl 4-(chloro(hydroxyimino)methyl)cyclohexanecarboxylate (0.900 g, 4.10 mmol) and but-2-yne-1,4-diol (0.370 g, 4.30 mmol) in 1,2-dichloroethane (41.0 ml) was added chloro(1,5-cyclooctadiene)(pentamethylcyclopentadienyl)ruthenium(II) (0.0778 g, 205 μmol) and triethylamine (0.713 ml, 5.12 mmol) at room temperature. The reaction mixture was stirred for 20 h. The solvent was evaporated. The residue was triturated in ethyl acetate (50 ml). The solids were removed by filtration and washed with ethyl acetate. The filtrate was concentrated in vacuo. Flash chromatography with n-heptane/ethyl acetate as eluent gave the title compound (0.758 g, 69%) as light brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513238B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-8806997d46b8432b848ed0e81dda8efa |
| Source note | uspto-grants-2013_08 |