HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535702Generated: October 29, 2026
Ether, ethyl ethynyl → 1-Ethoxyethene-2-boronic acid pinacol ester
https://huagongshe.com/reaction/535702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ether, ethyl ethynyl | HCID 61239 | — |
| Reactant | 4,4,5,5-Tetramethyl[1,3,2]dioxaborolane | HCID 2734768 | — |
| Catalyst | HCID 178420591 | HCID 178420591 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Ethoxyethene-2-boronic acid pinacol ester | HCID 21973908 | 78.13% |
Reaction Steps
Di(cyclopenta-2,4-dien-1-yl)zirconium(IV) chloride (0.685 g, 2.344 mmol) was added to a solution of 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (5.0 g, 39.1 mmol) in dichloromethane (15 mL) followed by ethoxyethyne (3.01 g, 43.0 mmol) at 0° C., and the mixture was stirred for 16 h at 25° C. Insoluble solids were filtered off, and filtrate was concentrated. Residue was partitioned between ethyl acetate and water. Organic layer was separated, washed with brine, dried over sodium sulphate, filtered and concentrated in vacuo to afford title compound (6.04 g, 78.13%) as oil. 1H NMR (400 MHz, CDCl3): δ 7.04 (d, J=14.0 Hz, 1H), 4.43 (d, J=14.8 Hz, 1H), 3.84 (q, J=7.2 Hz, 2H), 1.32-1.2 (m, 15H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859536B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-24ba5ff9fd66410eae84a84b65e16464 |
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| Source note | uspto-grants-2014_10 |
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