HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500260Generated: November 3, 2026
(4-Methoxyphenyl)boronic acid → Ethyl 2-(4-methoxyphenyl)thiazole-4-carboxylate
https://huagongshe.com/reaction/1500260
Participants
| Role | Name | HCID | Charge |
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| Reactant | (4-Methoxyphenyl)boronic acid | HCID 201262 | — |
| Reactant | Ethyl 2-bromo-1,3-thiazole-4-carboxylate | HCID 353965 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | Potassium phosphate, tribasic, monohydrate | HCID 22031701 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Product | Ethyl 2-(4-methoxyphenyl)thiazole-4-carboxylate | HCID 10400532 | — |
Reaction Steps
2-Bromo-thiazole-4-carboxylic acid ethyl ester (1.00 mmol, 236 mg), 4-methoxyphenylboronic acid (1.50 mmol, 228 mg), Pd2(DBA)3 (0.020 mmol, 18 mg), S-Phos (0.060 mmol, 25 mg) and potassium phosphate tribasic monohydrate (1.5 mmol, 0.35 g) were loaded into a Schlenk tube containing a stir bar. The Schlenk tube was capped with a rubber septum, evacuated and refilled with nitrogen. Toluene (2 mL) was added through the septum via a syringe and the Schlenk tube was sealed with a Teflon screw cap under a flow of nitrogen, and put into an oil bath at 100° C. The reaction was allowed to stir at 100° C. for 15 hours, then the reaction mixture was cooled to room temperature and filtered through celite. The filtrate was concentrated in vacuo and the resultant crude residue was purified using column chromatography on silica gel (eluent: Hexane/EtOAc (4:1)) to provide 2-(4-Methoxy-phenyl)-thiazole-4-carboxylic acid ethyl ester as a yellowish solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206142B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-4d36a83c1e664bcbb7c3d57263cbbcc8 |
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| Source note | uspto-grants-2015_12 |
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