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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537640Generated: November 2, 2026

Propargyl bromide → HCID 44475517, compound

https://huagongshe.com/reaction/537640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantHexaethylene GlycolHCID 17472—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44475517HCID 4447551754%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium hydride, 60% dispersion in mineral oil, (0.86 g, 21.4 mmol) was added in portions to the solution of hexaethylene glycol (5.5 g, 19.4 mmol) in anhydrous THF (40 mL) at 0° C. (FIG. 3). The reaction mixture was stirred at 0° C. for 15 minutes then propargyl bromide, 80% in toulene, (2.4 mL, 21.4 mmol) was added dropwise. The mixture was allowed to warm to room temperature and stirred for 3 hours. The formed sodium bromide was removed by filtration and the solvent was evaporated. The crude product was purified on SiO2 column using methanol/dichloromethane gradient 0-100% to yield 3.4 g (54%) of 1 as a colorless oil. 1H NMR (500 MHz, CDCl3): δ 2.45 (t, J=2.4 Hz, 1H), 2.74 (bs, 1H), 3.61-3.71 (m, 24H), 4.21 (d, J=2.4 Hz, 2H); 13C NMR (100.6 MHz, CDCl3): δ 58.4, 61.7, 69.1, 70.3-70.6, 72.5, 74.5, 79.7; MS ESI (m/z): [M+H]− calcd. for C15H29O7, 321.38. found 321.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865122B2
Source datasetuspto-grants-2014_10
ORD IDord-fa09c0f78ffd47b2b5a4c4a86977a29a
Source noteuspto-grants-2014_10