HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707606Generated: October 31, 2026
Ethyl 6-chloronicotinate → Ethyl 6-[2-(4,4,7-trimethylthiochroman-6-yl)ethynyl]nicotinate
https://huagongshe.com/reaction/1707606
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 6-chloronicotinate | HCID 2799611 | — |
| Reactant | 4,4,7-Trimethyl-6-ethynylthiochroman | HCID 15661128 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Ethyl 6-[2-(4,4,7-trimethylthiochroman-6-yl)ethynyl]nicotinate | HCID 9820494 | — |
Reaction Steps
A mixture of 86 mg (0.4 mmol) of 4,4,7-trimethyl-6-ethynylthiochroman, 85 mg (0.46 mmol) of ethyl 6-chloronicotinate and 0.8 ml of triethylamine was degassed under nitrogen and then treated with a mixture of 10 mg (0.05 mmol) of cuprous iodide and 20 mg (0.03 mmol) of bis(triphenylphosphine) palladium (II) chloride. The reaction mixture was heated at 55° C. under a nitrogen atmosphere for 18 hours. The mixture was then extracted with 1.5 ml of 40% ethyl acetate in hexanes and purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354752 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-1e048da13e0543c4ae40167e65d7c642 |
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| Source note | uspto-grants-1994_10 |
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