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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEther, ethyl ethynylHCID 61239—
Reactant4,4,5,5-Tetramethyl[1,3,2]dioxaborolaneHCID 2734768—
CatalystHCID 178420591HCID 178420591—
SolventDichloromethaneHCID 6344—
Product1-Ethoxyethene-2-boronic acid pinacol esterHCID 2197390878.13%

Reaction Conditions

Temperature25 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859536B2
Source datasetuspto-grants-2014_10
ORD IDord-24ba5ff9fd66410eae84a84b65e16464
Source noteuspto-grants-2014_10