HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459075Generated: October 30, 2026
Propargyl alcohol → HCID 58822792, compound
https://huagongshe.com/reaction/459075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 58822780 | HCID 58822780 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58822792 | HCID 58822792 | 32% |
Reaction Steps
A solution of (2S)-2-methoxy-3-(4-trifluoromethane-sulfonyloxy-phenyl)-propionic acid ethyl ester (0.861 g, 2.53 mmol), propargyl alcohol (0.88 mL, 15.18 mmol), triethylamine (1.41 mL, 10.12 mmol) and dichlorobis(triphenylphosphine)palladium (II) in 10 mL of dry DMF was heated to 90° C. for 2 hours. The reaction mixture was cooled to room temperature, diluted with 50 mL of water, and extracted with diethyl ether (3×30 mL). The combined organic layers were washed with 0.5 N HCl (2×20 mL) and brine (20 mL), dried (MgSO4), and concentrated. The residue purified by column chromatography (silica gel, hexanes/ethyl acetate 2:1, Rf0.17) to give a yellow-brown oil (0.211 g, 32%). 1H-NMR (200.15 MHz, CDCl3): δ 7.35 (d, 2H, J=8.1), 7.18 (d, 2H, J=8.1), 4.48 (s, 2H), 4.17 (q, 2H, J=7.3), 3.93 (dd, 1H, J=7.3, 5.7), 3.34 (s, 3H), 3.02 (s, 1H), 2.99 (d, 1H, J=2.2), 1.8 (s, 1H), 1.22 (t, 3H, J=7.3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192982B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-918ff3500f974fa3b6b0bcf686fd3edc |
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| Source note | uspto-grants-2007_03 |
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