HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799108Generated: October 25, 2026
Water → Ethyl 5-(3-methoxyprop-1-ynyl)-2-phenylthiazole-4-carboxylate
https://huagongshe.com/reaction/1799108
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 3-Methoxypropyne | HCID 69393 | — |
| Reactant | Ethyl 5-bromo-2-phenylthiazole-4-carboxylate | HCID 44558337 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Ethyl 5-(3-methoxyprop-1-ynyl)-2-phenylthiazole-4-carboxylate | HCID 67425118 | 88% |
Reaction Steps
Nitrogen was bubbled through a solution of Ethyl 5-bromo-2-phenylthiazole-4-carboxylate (13.1 g, 41.9 mmol) and methyl propargyl ether (7.1 mL, 83.9 mmol) in dimethoxyethane (DME) (200 mL). Dichlorobis(triphenylphosphine)palladium (II) (1.47 g, 2.2 mmol), copper (I) iodide (0.2 g, 1.1 mmol), and TEA (29 mL, 210 mmol) were added and the reaction mixture was heated at reflux for 16 h. The reaction mixture was cooled to room temperature, poured into H2O (200 mL) and extracted with EtOAc (2×200 mL). The combined organics were washed with brine, dried (MgSO4), and concentrated. The crude product was purified by MPLC eluting with pentane/EtOAc (0-50% gradient) to give ethyl 5-(3-methoxyprop-1-ynyl)-2-phenylthiazole-4-carboxylate as a tan solid (11 g, 88% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08343997B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-777aa7626cef49af9c9c8d2565fc433f |
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| Source note | uspto-grants-2013_01 |
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