HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942641Generated: November 2, 2026
Water → 2-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazole
https://huagongshe.com/reaction/1942641
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2-Bromothiazole | HCID 76430 | — |
| Reactant | 2-(3-Chloro-4-isopropoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | HCID 58494101 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazole | HCID 58494140 | 58.4% |
Reaction Steps
To a suspension of 2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (D69) (3 g), 2-bromo-1,3-thiazole (1.659 g) and Cs2CO3 (3.95 g) in 1,2-dimethoxyethane (DME) (40 mL)/water (10 mL) stirred under nitrogen at room temperature was added PdCl2(dppf)-CH2Cl2 adduct (661 mg) in one charge. The reaction vessel was sealed and heated under microwave at 120° C. for 2 h. After cooling the reaction, the reaction mixture was filtered and the filtrate was partitioned between ethyl acetate (150 mL) and saturated brine (50 mL). The organic phase was dried over sodium sulphate and evaporated in vacuo. The crude product was purified by column chromatography to give 2-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3-thiazole (D70) (1.5 g). MS (ES): C12H12ClNOS requires 253. found 254.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389508B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-efb2454fa1a8478ab4cfe6942cae6185 |
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| Source note | uspto-grants-2013_03 |
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