HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176250Generated: November 1, 2026
HCID 86706089, compound → HCID 86706088, compound
https://huagongshe.com/reaction/2176250
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 86706089 | HCID 86706089 | — |
| Reactant | 1,8-Diazabicycloundec-7ene | HCID 129662960 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86706088 | HCID 86706088 | 83% |
Reaction Steps
A solution of 2-(1-trifluoromethanesulfonyloxy-ethyl)-tetrahydro-pyran-2-carboxylic acid methyl ester (2.12 g, 3.3 mmol) in dichloromethane (5 mL) was stirred at room temperature under nitrogen. 1,8-Diazabicycloundec-7-ene (2.0 g, 2 mL, 13.2 mmol) was added and the reaction mixture was stirred at room temperature for 18 h. The reaction mixture was cooled to 0° C. and acidified to pH 2 with ice cold hydrochloric acid (2 M). The mixture was extracted with dichloromethane. The organic extracts were combined and washed with brine. The organic solution was filtered through a hydrophobic frit and the filtrate was evaporated. The residue was purified by silica gel chromatography using a gradient of pentane/diethyl ether 10:1 to 5:1 to afford the title compound (466 mg, 75% over two steps) as an oil. 1H NMR (300 MHz, CDCl3) δ 1.55-1.80 (m, 5H), 2.21-2.29 (m, 1H), 2.68-2.77 (m, 1H), 3.79 (s, 3H), 3.91-3.98 (m, 1H), 5.26 (dd, J=10.7, 0.9 Hz, 1H), 5.41 (dd, J=17.4, 1.1 Hz, 1H), 5.87 (dd, J=17.4, 10.7 Hz, 1H). LCMS (m/z) 193.2 [M+H], Tr=2.01 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062092B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-72a19f4013b442839f855202f505b8d0 |
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| Source note | uspto-grants-2015_06 |
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