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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377271Generated: October 31, 2026

Propargyl bromide → HCID 57887514, compound

https://huagongshe.com/reaction/2377271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantIsopropylethanediolHCID 7996—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57887514HCID 57887514—

Reaction Steps

To a 60% suspension of sodium hydride in mineral oil (2.3 g, 57.6 mmol) in tetrahydrofuran (65 mL) was added 2-isopropoxyethanol (3.0 g, 28.8 mmol) dropwise at about 0 C. The mixture was stirred for about 30 min, then propargyl bromide (3.2 mL, 28.8 mmol) was added dropwise and the mixture was stirred overnight while being allowed to warm to room temperature. The reaction was quenched by addition of water and the product was extracted with diethyl ether. The combined organic extracts were dried (MgSO4), filtered and the organic solvents were carefully distilled off at atmospheric pressure. The residue was purified by flash chromatography on silica gel using diethyl ether/n-pentane (1:6) as eluent to provide Example 613. 1H NMR (500 MHz, CDCl3): δ 1.17 (d, J=6.0 Hz, 6H), 2.42 (t, J=3.0 Hz, 1H), 3.57-3.76 (m, 5H), 4.21 (d, J=3.0 Hz, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468371B2
Source datasetuspto-grants-2008_12
ORD IDord-45b8d5c97bc047c0a4102adeb37d910c
Source noteuspto-grants-2008_12